N-Thio-anthranilamid compounds and their use as pesticides

ABSTRACT

N-Thio-anthranilamid compounds of formula (I) 
                         
wherein A is a group selected from A 1  and A 2 
 
                         
wherein the variables and the indices are as defined per the description, processes for preparing the compounds I, pesticidal compositions comprising compounds I, use of compounds I for the control of insects, acarids or nematodes, and methods for treating, controlling, preventing or protecting animals against infestation or infection by parasites by use of compounds of formula I.

This application is a National Stage application of International Application No. PCT/EP2006/063761 filed Jun. 30, 2006, which claims the benefit of U.S. Provisional Application No. 60/697,166, filed Jul. 7, 2005, the entire contents of each is hereby incorporated herein by reference.

The present invention relates to N-Thio-anthranilamid compounds of formula (I)

wherein

-   R¹ is hydrogen; or C₁-C₁₀-alkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, or     C₃-C₈-cycloalkyl, each of which is unsubstituted or substituted with     1 to 5 groups independently selected from halogen, cyano, nitro,     hydroxy, C₁-C₁₀-alkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-alkylsulfinyl,     C₂-C₁₀-alkoxycarbonyl, C₁-C₁₀-alkylamino, di(C₁-C₁₀-alkyl)amino and     C₃-C₈-cycloalkylamino; or C₁-C₁₀-alkylcarbonyl,     C₁-C₁₀-alkoxycarbonyl C₁-C₁₀-alkylaminocarbonyl,     di(C₁-C₁₀-alkyl)aminocarbonyl; -   A is a group selected from A¹ and A²

wherein # denotes the binding site;

-   R² and R³ each independently are R⁶, —C(=G)R⁷, —C(═NOR⁷)R⁷, —C(═NNR⁷     ₂)R⁷, —C(=G)OR⁷, —C(=G)NR⁷ ₂, —OC(=G)OR⁷, —OC(=G)OR⁷, —NR⁷C(=G)R⁷,     —N[C(=G)R⁷]2, —NR⁷C(=G)OR⁷, —C(=G)NR⁷—NR⁷ ₂, —C(=G)NR⁷—NR⁷[C(=G)R⁷],     —NR⁷—C(=G)NR⁷ ₂, —NR⁷—NR⁷C(=G)R⁷, —NR⁷—N[C(=G)R⁷]₂, —N[(C=G)R⁷]—NR⁷     ₂, —NR⁷—NR⁷—[(C=G)GR⁷], —NR⁷—[(C=G)NR⁷ ₂, —NR⁷[C═NR⁷]R⁷,     —NR⁷[(C═NR⁷)NR⁷ ₂, —O—NR⁷ ₂, —O—NR⁷(C=G)R⁷, —SO₂NR⁷ ₂, —NR⁷SO₂R⁷,     —SO₂₀R⁷, —OSO2R⁷, —NR⁷ ₂, —SR⁷, —SiR⁷ ₃, —PR⁷ ₂, —P(=G)R⁷, —SOR⁷,     —SO₂R⁷, —PG₂R⁷ ₂, or —PG₃R⁷ ₂; or -   R² and R³ together with the sulfur atom to which they are attached     form a saturated, partially unsaturated or unsaturated 3- to     8-membered ring which contains 1 to 4 heteroatoms selected from     oxygen, nitrogen, sulfur, which ring can be fused with one or two     saturated, partially unsaturated or unsaturated 5- to 6-membered     rings which may contain 1 to 4 heteroatoms selected from oxygen,     nitrogen, sulfur, wherein all of the above rings are unsubstituted     or substituted by any combination of 1 to 6 groups R⁸; -   G is oxygen or sulfur; -   R⁶ is C₁-C₂₀-alkyl, C₂-C₂₀-alkenyl, C₂-C₂₀-alkynyl,     C₃-C₈-cycloalkyl, C₃-C₈-cycloalkenyl, C₃-C₈-cycloalkynyl, phenyl,     naphthyl, biphenyl, or a saturated, partially unsaturated or     unsaturated 3- to 8-membered ring system which contains 1 to 4     heteroatoms selected from oxygen, nitrogen, sulfur, wherein all of     these groups are unsubstituted or substituted by any combination of     1 to 6 groups R⁸; -   R⁷ is hydrogen or R⁶; -   R⁸ is R⁹; or two groups R⁸ together with the atoms to which they are     attached form a saturated, partially unsaturated or unsaturated 3-     to 8-membered ring system which may contain 1 to 4     heteroatoms/heterogroups selected from oxygen, nitrogen, sulfur, SO     and SO₂, and which ring system is unsubstituted or substituted with     any combination of 1 to 6 groups R⁹. -   R⁹ is R¹⁰, R¹¹, —C(=G)R¹⁰, —C(═NOR¹⁰)R¹⁰, —C(═NNR¹⁰ ₂)R¹⁰,     —C(=G)OR¹⁰, —C(=G)NR¹⁰ ₂, —OC(=G)R¹⁰, —OC(=G)OR¹⁰, —NR¹⁰C(=G)R¹⁰,     —N[C(=G)R¹⁰]2, —NR¹⁰C(=G)OR¹⁰, —C(=G)NR¹⁰—NR¹⁰ ₂,     —C(=G)NR¹⁰—NR¹⁰[C(=G)R¹⁰], —NR¹⁰—C(=G)NR¹⁰ ₂, —NR¹⁰—NR¹⁰C(=G)R¹⁰,     —NR¹⁰—N[C(=G)R¹⁰]₂, —N[(C=G)R¹⁰]—NR¹⁰ ₂, —NR¹⁰—NR¹⁰[(C=G)GR¹⁰],     —NR¹⁰[(C=G)NR¹⁰ ₂, —NR¹⁰[C═NR¹⁰]R¹⁰, —NR¹⁰(C═NR¹⁰)NR¹⁰ ₂, —O—NR¹⁰ ₂,     —O—NR¹⁰(C=G)R¹⁰, —SO₂NR¹⁰ ₂, —NR¹⁰SO₂R¹⁰, —SO₂OR¹⁰, —OSO2R¹⁰, —OR¹⁰,     —NR¹⁰ ₂, —SR¹⁰, —SiR¹⁰ ₃, —PR¹⁰ ₂, —P(=G)R¹⁰, —SOR¹⁰, —SO₂R¹⁰,     —PG₂R¹⁰ ₂, —PG₃R¹⁰ ₂, or two groups R⁹ together are (=G), (═N—R¹⁰),     (═CR¹⁰ ₂), (═CHR¹⁰), or (═CH₂); -   R¹⁰ is C₁-C₁₀-alkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl,     C₃-C₈-cycloalkyl, C₄-C₈-cycloalkenyl, C₃-C₈-cycloalkyl-C₁-C₄-alkyl,     C₄-C₈-cycloalkenyl-C₁-C₄-alkyl, C₃-C₈-cycloalkyl-C₂-C₄-alkenyl,     C₄-C₈-cycloalkenyl-C₂-C₄-alkenyl, C₂-C₁₀-alkenyl-C₃-C₈-cycloalkyl,     C₂-C₁₀-alkynyl-C₃-C₈-cycloalkyl, C₁-C₁₀-alkyl-C₄-C₈-cycloalkenyl,     C₂-C₁₀-alkenyl-C₄-C₈-cycloalkenyl,     C₂-C₁₀-alkynyl-C₄-C₈-cycloalkenyl,     -   a saturated, partially unsaturated or unsaturated 3- to         8-membered ring system which contains 1 to 4 heteroatoms         selected from oxygen, nitrogen, sulfur, wherein the above groups         are unsubstituted or substituted with any combination of from 1         to 6 groups R¹¹; -   R¹¹ is halogen, cyano, nitro, hydroxy, mercapto, amino, formyl,     C₁-C₁₀-alkylcarbonyl, C₁-C₁₀-alkoxy, C₂-C₁₀-alkenyloxy,     C₂-C₁₀-alkynyloxy, C₁-C₁₀-haloalkoxy, C₃-C₁₀-haloalkenyloxy,     C₃-C₁₀-haloalkynyloxy, C₃-C₈-cycloalkoxy, C₄-C₈-cycloalkenyloxy,     C₃-C₈-halocycloalkoxy, C₄-C₈-halocycloalkenyloxy,     C₃-C₈-cycloalkyl-C₁-C₄-alkoxy, C₄-C₈-cycloalkenyl-C₁-C₄-alkoxy,     C₃-C₈-cycloalkyl-C₂-C₄-alkenyloxy,     C₄-C₈-cycloalkenyl-C₂-C₄-alkenyloxy, C₁-C₁₀-alkyl-C₃-C₈-cycloalkoxy,     C₁-C₁₀-alkenyl-C₃-C₈-cycloalkoxy, C₁-C₁₀-alkynyl-C₃-C₈-cycloalkoxy,     C₁-C₁₀-alkyl-C₃-C₈-cycloalkenyloxy,     C₁-C₁₀-alkenyl-C₃-C₈-cycloalkenyloxy, C₁-C₄-alkoxy-C₁-C₁₀-alkoxy,     C₁-C₄-alkoxy-C₂-C₁₀-alkenyloxy, mono- or di(C₁-C₁₀-alkyl)carbamoyl,     mono- or di(C₁-C₁₀-haloalkyl)carbamoyl, mono- or     di(C₃-C₈-cycloalkyl)carbamoyl, C₁-C₁₀-alkoxycarbonyl,     C₃-C₈-cycloalkoxycarbonyl, C₁-C₁₀-alkylcarbonyloxy, C₃-C₈-cyclo     alkylcarbonyloxy, C₁-C₁₀-haloalkoxycarbonyl,     C₁-C₁₀-haloalkylcarbonyloxy, C₁-C₁₀-alkanamido,     C₁-C₁₀-haloalkanamido, C₂-C₁₀-alkenamido, C₃-C₈-cycloalkanamido,     C₃-C₈-cycloalkyl-C₁-C₄-alkanamido, C₁-C₁₀-alkylthio,     C₂-C₁₀-alkenylthio, C₂-C₁₀-alkynylthio, C₁-C₁₀-haloalkylthio,     C₂-C₁₀-haloalkenylthio, C₂-C₁₀-haloalkynylthio,     C₃-C₈-cycloalkylthio, C₃-C₈-cycloalkenylthio,     C₃-C₈-halocycloalkylthio, C₃-C₈-halocycloalkenylthio,     C₃-C₈cycloalkyl-C₁-C₄-alkylthio, C₄-C₈-cycloalkenyl-C₁-C₄-alkylthio,     C₃-C₈-cycloalkylC₂-C₄-alkenylthio,     C₄-C₈-cycloalkenyl-C₂-C₄-alkenylthio,     C₁-C₁₀-alkyl-C₃-C₈-cycloalkylthio,     C₁-C₁₀-alkenyl-C₃-C₈-cycloalkylthio,     C₁-C₁₀-alkynyl-C₃-C₈-cycloalkylthio,     C₁-C₁₀-alkyl-C₃-C₈-cycloalkenylthio,     C₁-C₁₀-alkenyl-C₃-C₈-cycloalkenylthio, C₁-C₁₀-alkylsulfinyl,     C₂-C₁₀-alkenylsulfinyl, C₂-C₁₀-alkynylsulfinyl,     C₁-C₁₀-haloalkylsulfinyl, C₂-C₁₀-haloalkenylsulfinyl,     C₂-C₁₀-haloalkynylsulfinyl, C₃-C₈-cycloalkylsulfinyl,     C₃-C₈-cycloalkenylsulfinyl, C₃-C₈-halocycloalkylsulfinyl,     C₃-C₈-halocycloalkenylsulfinyl,     C₃-C₈-cycloalkyl-C₁-C₄-alkylsulfinyl,     C₄-C₈-cycloalkenyl-C₁-C₄-alkylsulfinyl,     C₃-C₈-cycloalkyl-C₂-C₄-alkenylsulfinyl,     C₄-C₈-cycloalkenyl-C₂-C₄-alkenylsulfinyl,     C₁-C₁₀-alkyl-C₃-C₈-cycloalkylsulfinyl,     C₁-C₁₀-alkenyl-C₃-C₈-cycloalkylsulfinyl,     C₁-C₁₀-alkynyl-C₃-C₈-cycloalkylsulfinyl,     C₁-C₁₀-alkyl-C₃-C₈-cycloalkenylsulfinyl,     C₁-C₁₀-alkenyl-C₃-C₈-cycloalkenylsulfinyl, C₁-C₁₀-alkylsulfonyl,     C₂-C₁₀-alkenylsulfonyl, C₂-C₁₀-alkynylsulfonyl,     C₁-C₁₀-haloalkylsulfonyl, C₂-C₁₀-haloalkenylsulfonyl,     C₂-C₁₀-haloalkynylsulfonyl, C₃-C₈-cycloalkylsulfonyl,     C₃-C₈-cycloalkenylsulfonyl, C₃-C₈-halocycloalkylsulfonyl,     C₃-C₈-halocycloalkenylsulfonyl,     C₃-C₈-cycloalkyl-C₁-C₄-alkylsulfonyl,     C₄-C₈-cycloalkenylC₁-C₄-alkylsulfonyl,     C₃-C₈-cycloalkyl-C₂-C₄-alkenylsulfonyl,     C₄-C₈-cycloalkenyl-C₂-C₄-alkenylsulfonyl,     C₁-C₁₀-alkyl-C₃-C₈-cycloalkylsulfonyl,     C₁-C₁₀-alkenyl-C₃-C₈-cycloalkylsulfonyl,     C₁-C₁₀-alkynyl-C₃-C₈-cycloalkylsulfonyl,     C₁-C₁₀-alkyl-C₃-C₈-cycloalkenylsulfonyl,     C₁-C₁₀-alkenyl-C₃-C₈-cycloalkenylsulfonyl, di(C₁-C₁₀-alkyl)amino,     C₁-C₁₀-alkylamino, C₂-C₁₀-alkenylamino, C₂-C₁₀-alkynylamino,     C₁-C₁₀-alkyl-C₂-C₁₀-alkenylamino, C₁-C₁₀-alkyl-C₂-C₁₀-alkynylamino,     C₁-C₁₀-haloalkylamino, C₂-C₁₀-haloalkenylamino,     C₂-C₁₀-haloalkynylamino, C₃-C₈-cycloalkylamino,     C₃-C₈-cycloalkenylamino, C₃-C₈-halocycloalkylamino,     C₃-C₈-halocycloalkenylamino, C₃-C₈-cycloalkyl-C₁-C₄-alkylamino,     C₄-C₈-cycloalkenyl-C₁-C₄-alkylamino,     C₃-C₈-cycloalkyl-C₂-C₄-alkenylamino,     C₄-C₈-cycloalkenyl-C₂-C₄-alkenylamino,     C₁-C₁₀-alkyl-C₃-C₈-cycloalkylamino,     C₁-C₁₀-alkenyl-C₃-C₈-cycloalkylamino,     C₁-C₁₀-alkynyl-C₃-C₈-cycloalkylamino,     C₁-C₁₀-alkyl-C₃-C₈-cycloalkenylamino,     C₁-C₁₀-alkenyl-C₃-C₈-cycloalkenylamino, tri(C₁-C₁₀-alkyl)silyl,     aryl, aryloxy, arylthio, arylamino, aryl-C₁-C₄-alkoxy,     aryl-C₃-C₄-alkenyloxy, aryl-C₁-C₄-alkylthio, aryl-C₂-C₄-alkenylthio,     aryl-C₁-C₄-alkylamino, aryl-C₃-C₄-alkenylamino, triarylsilyl,     wherein aryl is phenyl, naphthyl or biphenyl, or     -   a saturated, partially unsaturated or unsaturated 3- to         8-membered ring system which contains 1 to 4 heteroatoms         selected from oxygen, nitrogen, sulfur, wherein these aryl and         these heterocyclic ringsystems are unsubstituted or substituted         with any combination of from 1 to 6 groups selected from         halogen, cyano, nitro, amino, hydroxy, mercapto, C₁-C₄-alkyl,         C₁-C₄-haloalkyl, C₃-C₈-cycloalkyl, C₁-C₄-alkoxy,         C₁-C₄-haloalkoxy, C₁-C₄-alkylthio, C₁-C₄-haloalkylthio,         di(C₁-C₄-alkyl)amino, C₁-C₄-alkylamino, C₁-C₄-haloalkylamino,         formyl and C₁-C₄-alkylcarbonyl; -   R⁴ is NR¹²R¹³;     -   R¹² and R¹³ are each independently hydrogen; or C₁-C₂₀-alkyl,         C₂-C₂₀-alkenyl or C₂-C₂₀-alkynyl, each of which is unsubstituted         or substituted with any combination of 1 to 6 groups selected         from C₁-C₄-alkoxy, C₁-C₄-alkylthio, cyano, nitro, formyl,         C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxycarbonyl,         C₁-C₄-alkylaminocarbonyl, di(C₁-C₄-alkyl)aminocarbonyl,         C₁-C₄-alkylsulfinyl, C₁-C₄alkylsulfonyl, C₃-C₈-cycloalkyl, and         phenyl, wherein phenyl itself is unsubstituted or substituted by         1 to 4 substituents selected from halogen, C₁-C₄-alkyl,         C₁-C₄-alkoxy, C₁-C₄-fluoroalkyl, C₁-C₄-alkyloxycarbonyl,         trifluoromethylsulfonyl, formyl, nitro and cyano; or     -   C₁-C₂₀-haloalkyl, C₂-C₂₀-haloalkenyl, C₂-C₂₀-haloalkynyl,         C₅-C₁₀-cycloalkenyl, or a saturated or partially unsaturated or         unsaturated 3- to 8-membered ring system which contains 1 to 4         heteroatoms selected from oxygen, nitrogen, sulfur, or phenyl or         naphthyl, wherein this ring system and phenyl or naphthyl         themselves are unsubstituted or substituted by 1 to 4         substituents selected from halogen, C₁-C₄-alkyl, C₁-C₄-alkoxy,         C₁-C₄-fluoroalkyl, C₁-C₄-alkyloxycarbonyl,         trifluoromethylsulfonyl, formyl, nitro and cyano; or     -   R¹² and R¹³ together with the nitrogen atom to which they are         attached form a saturated or partially unsaturated 5- to         8-membered heterocycle which besides the one nitrogen atom         contains 0 to 2 further heteroatoms selected from oxygen,         nitrogen, sulfur, and may contain 1 or 2 carbonyl groups or         thiocarbonyl groups and which is unsubstituted or substituted by         from 1 to 4 groups selected from C₁-C₄-alkyl, C₁-C₄-alkoxy and         C₁-C₄-haloalkyl; -   R⁵ is hydrogen; or C₁-C₂₀-alkyl, C₂-C₂₀-alkenyl, C₂-C₂₀-alkynyl,     C₁-C₄-alkylcarbonyl, C₁-C₄-alkylaminocarbonyl, C₁-C₄-alkoxycarbonyl,     each of which is unsubstituted or substituted by from 1 to 6 groups     selected from C₁-C₄-alkoxy, C₁-C₄-alkylthio, cyano, nitro, formyl,     C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxycarbonyl, C₁-C₄-alkylaminocarbonyl,     di(C₁-C₄-alkyl)aminocarbonyl, C₁-C₄-alkylsulfinyl,     C₁-C₄-alkylsulfonyl, C₃-C₈-cycloalkyl, and phenyl, wherein phenyl     itself is unsubstituted or substituted by 1 to 4 substituents     selected from halogen, C₁-C₄-alkyl, C₁-C₄-alkoxy, C₁-C₄-fluoroalkyl,     C₁-C₄-alkyloxycarbonyl, trifluoromethylsulfonyl, formyl, nitro and     cyano; or     -   C₁-C₂₀-haloalkyl, C₂-C₂₀-haloalkenyl, C₂-C₂₀-haloalkynyl,         C₅-C₁₀-cycloalkenyl, or a saturated or partially unsaturated or         unsaturated 3- to 8-membered ring system which contains 1 to 4         heteroatoms selected from oxygen, nitrogen, sulfur, or phenyl or         naphthyl, wherein this ring system and phenyl or naphthyl         themselves are unsubstituted or substituted by 1 to 4         substituents selected from halogen, C₁-C₄-alkyl, C₁-C₄-alkoxy,         C₁-C₄-fluoroalkyl, C₁-C₄-alkyloxycarbonyl,         trifluoromethylsulfonyl, formyl, nitro and cyano; -   Q¹ and Q² each independently are hydrogen, halogen, cyano, SCN,     nitro, hydroxy, C₁-C₁₀-alkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl,     C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl,     C₃-C₈-halocycloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy,     C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio, C₁-C₁₀-alkylsulfinyl,     C₁-C₁₀-haloalkylsulfinyl, C₁-C₁₀-alkylsulfonyl,     C₁-C₁₀-haloalkylsulfonyl, C₁-C₁₀-alkylsulfonyloxy,     C₁-C₁₀-haloalkylsulfonyloxy, C₁-C₁₀-alkylamino,     di(C₁-C₁₀-alkyl)amino, C₃-C₈-cyclalkylamino, alkylcarbonyl,     C₁-C₁₀-alkoxycarbonyl, C₁-C₁₀-alkylaminocarbonyl,     di(C₁-C₁₀-alkyl)aminocarbonyl, or tri(C₁-C₁₀)-alkylsilyl, or -   Q¹ and Q² are each independently phenyl, benzyl or phenoxy, wherein     each ring is un-substituted or substituted with any combination of     from 1 to 3 substituents independently selected from the group     halogen, cyano, nitro, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl,     C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl,     C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl,     C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio,     C₁-C₁₀-alkylsulfinyl, C₁-C₁₀alkylsulfonyl, C₁-C₁₀-alkylamino,     di(C₁-C₁₀-alkyl)amino, C₃-C₈-cycloalkylamino,     C₁-C₁₀-alkyl-C₃-C₈-cycloalkylamino, C₁-C₁₀-alkylcarbonyl,     C₁-C₁₀-alkoxycarbonyl, C₁-C₁₀-alkylaminocarbonyl,     di(C₁-C₁₀-alkyl)aminocarbonyl and tri(C₁-C₁₀)-alkylsilyl; -   Q³ is halogen; or C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl,     C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl,     C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl,     C₁-C₁₀-alkyl-C₃-C₈-cycloalkyl, C₁-C₁₀-haloalkyl-C₃-C₈-cycloalkyl,     each unsubstituted or independently substituted with 1 to 2 groups     selected from cyano, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy,     C₁-C₁₀-haloalkylthio, C₁-C₁₀-alkylsulfinyl,     C₁-C₁₀-haloalkylsulfinyl, C₁-C₁₀-alkylsulfonyl,     C₁-C₁₀-haloalkylsulfonyl, and C₁-C₁₀-alkoxycarbonyl; or -   Q³ is OR¹⁴, S(O)_(q)R¹⁴, NR₁₅R₁₆, OS(O)₂R¹⁷, NR¹⁶S(O)₂R¹⁷, C(S)NH₂,     C(R¹⁸)═NOR¹⁸, C₃-C₈-cycloalkyl-C₁-C₄-alkyl,     C₁-C₁₀-alkylaminothiocarbonyl, or di(C₁-C₁₀-alkyl)aminothiocarbonyl;     -   R¹⁴ is C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl,         C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl,         C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl,         C₃-C₈-cycloalkyl-C₁-C₄-alkyl, C₁-C₄-alkyl-C₃-C₈-cycloalkyl,         C₃-C₈-halocycloalkyl-C₁-C₄-alkyl,         C₁-C₄-haloalkyl-C₃-C₈-cycloalkyl, or C₁-C₁₀haloalkylcarbonyl,         each unsubstituted or substituted with 1 R¹⁹;     -   R¹⁵ is C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl,         C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl,         C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl,         C₁-C₄-alkyl-C₃-C₈-cycloalkyl, C₁-C₄-haloalkyl-C₃-C₈-cycloalkyl,         or C₁-C₁₀-haloalkylcarbonyl, each unsubstituted or substituted         with 1 R¹⁹;     -   R¹⁶ is hydrogen; or C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl,         C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl,         C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl,         C₁-C₄-alkyl-C₃-C₈-cycloalkyl, or         C₁-C₄-haloalkyl-C₃-C₈-cycloalkyl, each unsubstituted or         substituted with 1 R¹⁹;     -   R¹⁷ is C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl,         C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl,         C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl,         C₁-C₄-alkyl-C₃-C₈-cycloalkyl, or         C₁-C₄-haloalkyl-C₃-C₈-cycloalkyl, each unsubstituted or         substituted with 1 R¹⁹;         -   R¹⁹ is cyano, nitro, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy,             C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio,             C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-haloalkylsulfinyl,             C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-haloalkylsulfonyl,             C₁-C₁₀-alkoxycarbonyl, C₁-C₁₀-alkylamino, or             di(C₁-C₁₀-alkyl)amino; or         -   R¹⁹ is phenyl or a heteroaromatic 5- or 6-membered ring             which contains 1 to 4 heteroatoms selected from oxygen,             nitrogen, sulfur, the phenyl radical and the heteroaromatic             ring being unsubstituted or substituted with any combination             of from 1 to 3 groups selected from halogen, cyano, nitro,             C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl,             C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl,             C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₁₀-alkoxy,             C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-alkylsulfinyl,             C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-alkylamino,             di(C₁-C₁₀-alkyl)amino, C₃-C₈-cycloalkylamino,             C₁-C₁₀-alkylC₃-C₈-cycloalkylamino, C₁-C₁₀-alkylcarbonyl,             C₁-C₁₀-alkoxycarbonyl, C₁-C₁₀-alkylaminocarbonyl,             di(C₁-C₁₀-alkyl)aminocarbonyl and tri(C₁-C₁₀)-alkylsilyl;     -   R¹⁸ is the same or different: hydrogen, C₁-C₁₀-alkyl, or         C₁-C₁₀-haloalkyl; -   q is 0, 1 or 2; -   Q⁴ is halogen, cyano, nitro, hydroxy, COOH, C(O)NH₂, C₁-C₁₀-alkyl,     C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl,     C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl,     C₃-C₈-halocycloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy,     C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio, C₁-C₁₀-alkylsulfinyl,     C₁-C₁₀-haloalkylsulfinyl, C₁-C₁₀-alkylsulfonyl,     C₁-C₁₀-haloalkylsulfonyl, C₁-C₁₀-alkylamino, di(C₁-C₁₀-alkylamino,     C₃-C₈-cycloalkylamino, C₁-C₁₀-alkylcarbonyl, C₁-C₁₀-alkoxycarbonyl     C₁-C₁₀-alkylaminocarbonyl, di(C₁-C₁₀-alkyl)aminocarbonyl or     tri(C₁-C₁₀)-alkylsilyl; or -   Q⁴ is phenyl, benzyl, benzyloxy, phenoxy, a 5- or 6-membered     heteroaromatic ring which contains 1 to 4 heteroatoms selected from     oxygen, nitrogen, sulfur or an aromatic 8-, 9- or 10-membered fused     heterobicyclic ring system which contains 1 to 4 heteroatoms     selected from oxygen, nitrogen, sulfur, wherein each of the above     ring systems is unsubstituted or substituted with any combination of     from 1 to 3 groups selected from halogen, cyano, nitro,     C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl,     C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl,     C₃-C₈-halocycloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy,     C₁-C₁₀-alkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-alkylsulfonyl,     C₁-C₁₀-alkylamino, di(C₁-C₁₀-alkyl)amino, C₃-C₈-cycloalkylamino,     C₁-C₁₀-alkyl-C₃-C₈-cycloalkylamino, C₁-C₁₀-alkylcarbonyl,     C₁-C₁₀-alkoxycarbonyl, C₁-C₁₀-alkylaminocarbonyl,     di(C₁-C₁₀-alkyl)aminocarbonyl and tri(C₁-C₁₀)-alkylsilyl; -   X and Y are each independently oxygen or sulfur; -   V and V′ are each independently N or CQ²; -   W is N, CH or CQ⁴; -   m is 0, 1 or 2; -   n is 0 or 1; -   p is 0, 1, 2, 3, or 4; -   or the enantiomers or salts or N-oxides thereof.

In addition, the present invention relates to processes for preparing the compounds I, pesticidal compositions comprising compounds I and methods for the control of insects, acarids or nematodes by contacting the insect, acarid or nematode or their food supply, habitat or breeding grounds with a pesticidally effective amount of compounds or compositions of formula I.

Moreover, the present invention also relates to a method of protecting growing plants from attack or infestation by insects or acarids by applying to the foliage of the plants, or to the soil or water in which they are growing, with a pesticidally effective amount of compositions or compounds of formula I.

This invention also provides a method for treating, controlling, preventing or protecting animals against infestation or infection by parasites which comprises orally, topically or parenterally administering or applying to the animals a parasiticidally effective amount of compositions or compounds of formula I.

In spite of the commercial insecticides, acaricides and nematicides available today, damage to crops, both growing and harvested, caused by insects and nematodes still occurs. Therefore, there is continuing need to develop new and more effective insecticidal, acaricidal and nematicidal agents.

It was therefore an object of the present invention to provide new pesticidal compositions, new compounds and new methods for the control of insects, acarids or nematodes and of protecting growing plants from attack or infestation by insects, arachnids or nematodes.

We have found that these objects are achieved by the compositions and the compounds of formula I. Furthermore, we have found processes for preparing the compounds of formula I.

Anthranilamide compounds have been described in a number of patent applications (WO 01/70671, WO 03/015518, WO 03/015519, WO 04/046129). N-Thioanthranilamide compounds have not been described in the prior art.

Compounds of the formula (I-1) wherein X and Y are oxygen and the other substituents are as defined above for formula (I)

can be prepared by reacting a carboxylic acid of the formula (II)

wherein the variables are as defined for formula (I) in the form of an activated derivative of this acid in the presence of a base with a compound of the formula A¹-H or A²-H, respectively, wherein the variables are as defined for formula (I).

Suitable activated derivatives of the acid which may be used are, for example, anhydrides, azolides, or acid halides.

The activated derivatives of the acid can be obtained according to procedures known in the art, e.g. as listed in “Comprehensive Organic Reactions” VCH Publishers 1989, for the anhydride: pp 965-66, for the acid halides: p 978.

Suitable bases are, for example, amines such as triethylamine, diisopropylethylamine, pyridine or lutidine or else alkali hydrides, hydroxides, carbonates, or alkaline earth metal hydroxides, carbonates or bicarbonates.

The amount of the base that can be used in the reaction is usually 1 to 5 moles relative to 1 mole of compound (II).

The reaction is advantageously carried out in an inert solvent such as dichloromethane, chloroform, carbon tetrachloride, benzene, toluene, diethyl ether or tetrahydrofurane, or mixtures of these solvents, in a temperature range between 0° C. and 100° C., preferably between 20° C. and 50° C.

A preferred procedure for the preparation of specific compounds of formula (I-1) involves the reaction of A¹-H or A²-H, respectively, with a benzoxazinone of formula (III)

wherein the variables are as defined for formula (I). Typical procedures involve combination of the compounds A¹-H or A²-H with the benzoxazinone of formula (III) in inert solvent such as dichloromethane, chloroform, carbon tetrachloride, benzene, toluene, diethyl ether or tetrahydrofurane, or mixtures of these solvents, in a temperature range between 0° C. and 100° C., preferably between 20° C. and 50° C. Addition of a base can be beneficial. Suitable bases are, for example, tertiary amines such as triethylamine, diisopropylethylamine, pyridine or lutidine or else alkali hydrides, hydroxides, carbonates, or alkaline earth metal hydroxides, carbonates or bicarbonates. The amount of the base that can be used in the reaction is usually 1 to 5 moles relative to 1 mole of compound (III).

Benzoxazinones are well documented in the chemical literature and are available via known methods that involve the coupling of either an anthranilic acid or an isatoic anhydride with an acid chloride. For references to the synthesis and chemistry of benzoxazinones see Jakobsen et al, Bioorganic and Medicinal Chemistry, 2000, 8, 2095-2103 and references cited therein. See also Coppola, J. Heterocyclic Chemistry, 1999, 36, 563-588. The benzoxazinones of formula III can also be prepared according to the procedures described in WO 04/046129 or WO 04/011447 as well as according to references cited therein and suitable modifications thereof.

Compounds of the formula (I-2) in which A is A¹, n is 0, X and Y are oxygen and the other variables are as defined for formula (I),

can be prepared by reacting an amide of the formula (IV)

wherein the variables are as defined for formula (I), with a sulfoxide of the formula (V),

in the presence of a condensating agent, giving the compounds of formula (I-2) with elimination of water. Suitable condensing agents are, for example, phosphorous oxychloride, phosphorous (V) oxide, methanesulfonyl chloride, sulfuryl chloride, sulfur trichloride, boron triflouride, dicyclohexylcarbodiimide, aryl cyanates or acid anhydrides, preferably trifluoroacetic anhydride or trifluoromethanesulfonic anhydride.

In the compounds of the formula (I) prepared as described above in which A is A¹, n is 0, X and Y are oxygen and the other variables are as defined for formula (I) the sulfur atom can be oxidized to give the respective compounds of the formula (I) in which n is 1. Suitable oxidizing agents are, for example, sodium periodate or organic peracids, such as 3-chloroperbenzoic acid, see e.g. Houben-Weyl, Methoden der Organischen Chemie, Bd. E11, p. 1299 ff., G. Thieme Verlag, Stuttgart 1985.

The carboxylic acids of formula (II) and the amides of formula (IV) can be prepared, for example, according to the procedures described in WO 04/046129 or WO 04/011447 as well as according to references cited therein and suitable modifications thereof.

After completion of the reaction, the compounds of formula I can be isolated by employing conventional methods such as adding the reaction mixture to water, extracting with an organic solvent, concentrating the extract an the like. The isolated compound (I) can be purified by a technique such as chromatography, recrystallization and the like, if necessary.

Compounds of formula A¹-H can be prepared according to procedures known in the art, e.g. as described in U.S. Pat. No. 6,136,983 and references cited therein.

Compounds of formula A²-H can be prepared according to procedures known in the art, e.g. as described in WO 03/097589 and references cited therein.

Sulfoxides of formula V can be obtained according to procedures known in the art, e.g. as described in J. March, Advanced Organic Chemistry, 4th Edition, Wiley, 1992, p. 1297.

Compounds of formula I, II, III, IV, V, and compounds A¹-H and A²-H which cannot be prepared according to the above procedures can be prepared according to suitable modifications of the above procedures.

The preparation of the compounds of formula I above may lead to them being obtained as isomer mixtures. If desired, these can be resolved by the methods customary for this purpose, such as crystallization or chromatography, also on optically active adsorbate, to give the pure isomers.

Agronomically acceptable salts of the compounds I can be formed in a customary manner, e.g. by reaction with an acid of the anion in question.

In this specification and in the claims, reference will be made to a number of terms that shall be defined to have the following meanings:

“Salt” as used herein includes adducts of compounds I with maleic acid, dimaleic acid, fumaric acid, difumaric acid, methane sulfenic acid, methane sulfonic acid, and succinic acid. Moreover, included as “salts” are those that can form with, for example, amines, metals, alkaline earth metal bases or quaternary ammonium bases, including zwitterions. Suitable metal and alkaline earth metal hydroxides as salt formers include the salts of barium, aluminum, nickel, copper, manganese, cobalt zinc, iron, silver, lithium, sodium, potassium, magnesium or calcium. Additional salt formers include chloride, sulfate, acetate, carbonate, hydride, and hydroxide. Desirable salts include adducts of compounds I with maleic acid, dimaleic acid, fumaric acid, difumaric acid, and methane sulfonic acid.

“Halogen” will be taken to mean fluoro, chloro, bromo and iodo.

The term “alkyl” as used herein refers to a branched or unbranched saturated hydrocarbon group having 1 to 10 carbon atoms, such as, and preferably, C₁-C₆-alkyl, for example methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl, 1-ethylpropyl, hexyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 2-ethylbutyl, 1,1,2-trimethylpropyl, 1,2,2-trimethylpropyl, 1-ethyl-1-methylpropyl and 1-ethyl-2-methylpropyl.

The term “haloalkyl” as used herein refers to a straight-chain or branched alkyl group having 1 to 10 carbon atoms (as mentioned above), where some or all of the hydrogen atoms in these groups may be replaced by halogen atoms as mentioned above, for example C₁-C₂-haloalkyl, such as chloromethyl, bromomethyl, dichloromethyl, trichloromethyl, fluoromethyl, difluoromethyl, trifluoromethyl, chlorofluoromethyl, dichlorofluoromethyl, chlorodifluoromethyl, 1-chloroethyl, 1-bromoethyl, 1-fluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, 2-chloro-2-fluoroethyl, 2-chloro-2,2-difluoroethyl, 2,2-dichloro-2-fluoroethyl, 2,2,2-trichloroethyl and pentafluoroethyl;

Similarly, “alkoxy” and “alkylthio” refer to straight-chain or branched alkyl groups having 1 to 10 carbon atoms (as mentioned above) bonded through oxygen or sulfur linkages, respectively, at any bond in the alkyl group. Examples include methoxy, ethoxy, propoxy, isopropoxy, methylthio, ethylthio, propylthio, isopropylthio, and n-butylthio.

Similarly, “alkylamino” refers to a nitrogen atom which carries 1 or 2 straight-chain or branched alkyl groups having 1 to 10 carbon atoms (as mentioned above) which may be the same or different. Examples include methylamino, dimethylamino, ethylamino, diethylamino, methylethylamino, isopropylamino, or methylisopropylamino.

Similarly, “alkylsulfinyl” and “alkylsulfonyl” refer to straight-chain or branched alkyl groups having 1 to 10 carbon atoms (as mentioned above) bonded through —S(═O)— or —S(═O)₂-linkages, respectively, at any bond in the alkyl group. Examples include methylsulfinyl and methylsulfonyl.

The term “alkylcarbonyl” refers to straight-chain or branched alkyl groups having 1 to 10 carbon atoms (as mentioned above) bonded through a —C(═O)— linkage, respectively, at any bond in the alkyl group. Examples include acetyl, propionyl, buturyl, or 2-methylbuturyl.

The term “alkenyl” as used herein intends a branched or unbranched unsaturated hydrocarbon group having 2 to 6 carbon atoms and a double bond in any position, such as ethenyl, 1-propenyl, 2-propenyl, 1-methyl-ethenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-methyl-1-propenyl, 2-methyl-1-propenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl; 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1-methyl-1-butenyl, 2-methyl-1-butenyl, 3-methyl-1-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, 1,1-dimethyl-2-propenyl, 1,2-dimethyl-1-propenyl, 1,2-dimethyl-2-propenyl, 1-ethyl-1-propenyl, 1-ethyl-2-propenyl, 1-hexenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, 1-methyl-1-pentenyl, 2-methyl-1-pentenyl, 3-methyl-1-pentenyl, 4-methyl-1-pentenyl, 1-methyl-2-pentenyl, 2-methyl-2-pentenyl, 3-methyl-2-pentenyl, 4-methyl-2-pentenyl, 1-methyl-3-pentenyl, 2-methyl-3-pentenyl, 3-methyl-3-pentenyl, 4-methyl-3-pentenyl, 1-methyl-4-pentenyl, 2-methyl-4-pentenyl, 3-methyl-4-pentenyl, 4-methyl-4-pentenyl, 1,1-dimethyl-2-butenyl, 1,1-dimethyl-3-butenyl, 1,2-dimethyl-1-butenyl, 1,2-dimethyl-2-butenyl, 1,2-dimethyl-3-butenyl, 1,3-dimethyl-1-butenyl, 1,3-dimethyl-2-butenyl, 1,3-dimethyl-3-butenyl, 2,2-dimethyl-3-butenyl, 2,3-dimethyl-1-butenyl, 2,3-dimethyl-2-butenyl, 2,3-dimethyl-3-butenyl, 3,3-dimethyl-1-butenyl, 3,3-dimethyl-2-butenyl, 1-ethyl-1-butenyl, 1-ethyl-2-butenyl, 1-ethyl-3-butenyl, 2-ethyl-1-butenyl, 2-ethyl-2-butenyl, 2-ethyl-3-butenyl, 1,1,2-trimethyl-2-propenyl, 1-ethyl-1-methyl-2-propenyl, 1-ethyl-2-methyl-1-propenyl and 1-ethyl-2-methyl-2-propenyl;

The term “alkynyl” as used herein refers to a branched or unbranched unsaturated hydrocarbon group containing at least one triple bond, such as ethynyl, propynyl, 1-butynyl, 2-butynyl, and the like.

A saturated, partially unsaturated or unsaturated 3- to 8-membered ring system which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, is a ring system wherein two oxygen atoms must not be in adjacent positions and wherein at least 1 carbon atom must be in the ring system e.g. thiophen, furan, pyrrol, thiazol, oxazol, imidazol, isothiazol, isoxazol, pyrazol, 1,3,4-oxadiazol, 1,3,4-thiadiazol, 1,3,4-triazol, 1,2,4-oxadiazol, 1,2,4-thiadiazol, 1,2,4-triazol, 1,2,3-triazol, 1,2,3,4-tetrazol, benzo[b]thiophen, benzo[b]furan, indol, benzo[c]thiophen, benzo[c]furan, isoindol, benzoxazol, benzothiazol, benzimidazol, benzisoxazol, benzisothiazol, benzopyrazol, benzothiadiazol, benzotriazol, dibenzofuran, dibenzothiophen, carbazol, pyridin, pyrazin, pyrimidin, pyridazin, 1,3,5-triazin, 1,2,4-triazin, 1,2,4,5-tetrazin, chinolin, isochinolin, chinoxalin, chinazolin, cinnolin, 1,8-naphthyridin, 1,5-naphthyridin, 1,6-naphthyridin, 1,7-naphthyridin, phthalazin, pyridopyrimidin, purin, pteridin, 4H-chinolizin, piperidin, pyrrolidin, oxazolin, tetrahydrofuran, tetrahydropyran, isoxazolidin or thiazolidin.

A saturated, partially unsaturated or unsaturated 3- to 8-membered ring system which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur also is e.g.

a saturated, partially unsaturated or unsaturated 5- or 6-membered heterocycle which contains 1 to 4 heteroatoms selected from oxygen, nitrogen and sulfur, such as pyridine, pyrimidine, (1,2,4)-oxadiazole, (1,3,4)-oxadiazole, pyrrole, furan, thiophene, oxazole, thiazole, imidazole, pyrazole, isoxazole, 1,2,4-triazole, tetrazole, pyrazine, pyridazine, oxazoline, thiazoline, tetrahydrofuran, tetrahydropyran, morpholine, piperidine, piperazine, pyrroline, pyrrolidine, oxazolidine, thiazolidine, oxirane or oxetane; or a saturated, partially unsaturated or unsaturated 5- or 6-membered heterocycle which contains 1 nitrogen atom and 0 to 2 further heteroatoms selected from oxygen, nitrogen and sulfur, preferably from oxygen and nitrogen, such as piperidine, piperazin and morpholine.

Preferably, this ring system is a saturated, partially unsaturated or unsaturated 3- to 6-membered ring system which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, wherein two oxygen atoms must not be in adjacent positions and wherein at least 1 carbon atom must be in the ring system.

Most preferably, this ring system is a radical of pyridine, pyrimidine, (1,2,4)-oxadiazol, 1,3,4-oxadiazol, pyrrol, furan, thiophen, oxazol, thiazol, imidazol, pyrazol, isoxazol, 1,2,4-triazol, tetrazol, pyrazin, pyridazin, oxazolin, thiazolin, tetrahydrofuran, tetrahydropyran, morpholin, piperidin, piperazin, pyrrolin, pyrrolidin, oxazolidin, thiazolidin, oxiran or oxetan.

Tri(C₁-C₁₀)alkylsilyl refers to a silicon atom having 3 straight-chain or branched C₁-C₁₀-alkyl groups as defined above which may be the same or different. Examples include trimethylsilyl, triethylsilyl, triphenylsilyl or triisopropylsilyl.

Cycloalkyl: monocyclic 3- to 6-, or 8-membered saturated carbon atom rings, e.g. C₃-C₈-cycloalkyl such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl.

With respect to the intended use of the compounds of formula I, particular preference is given to the following meanings of the substituents, in each case on their own or in combination:

A compound of formula I wherein R¹ is hydrogen, C₁-C₆-alkyl, cyano, C₁-C₆-alkylsulfonyl, or C₂-C₆-alkoxycarbonyl, preferably hydrogen or C₁-C₄-alkyl, most preferably hydrogen.

A compound of formula I wherein A is A¹.

A compound of formula I wherein A is A².

A compound of formula I wherein R² and R³ each independently are R⁶, —C(═O)R⁷, —C(═NOR⁷)R⁷, —C(═NNR⁷ ₂)R⁷, —C(═O)OR⁷, —C(═O)NR⁷ ₂, —OC(═O)R⁷, —OC(═O)OR⁷, C(═O)NR⁷—NR⁷ ₂, —C(═O)NR⁷—NR⁷[C(═O)R⁷], or R² and R³ together with the sulfur atom to which they are attached form a saturated, partially unsaturated or unsaturated 3- to 8-membered ring which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, which ring can be fused with one or two saturated, partially unsaturated or unsaturated 5- to 6-membered rings which may contain 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, wherein all of the above rings are unsubstituted or substituted by any combination of 1 to 6 groups R⁸.

More preferably, R² and R³ each independently are R⁶ or R² and R³ together with the sulfur atom to which they are attached form a saturated, partially unsaturated or unsaturated 3- to 8-membered ring which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, which ring can be fused with one or two saturated, partially unsaturated or unsaturated 5- to 6-membered rings which may contain 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, wherein all of the above rings are unsubstituted or substituted by any combination of 1 to 6 groups R⁸.

Even more preferred are compounds of formula I wherein R² and R³ each independently are R⁶, preferably hydrogen, C₁-C₂₀-alkyl, C₂-C₂₀-alkenyl, C₂-C₂₀-alkynyl, C₃-C₈-cycloalkyl, C₃-C₈-cycloalkenyl, C₃-C₈-cycloalkynyl, phenyl, naphthyl, biphenyl, or a saturated, partially unsaturated or unsaturated 3- to 8-membered ring which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, wherein all of these groups are unsubstituted or substituted by any combination of 1 to 6 groups R⁹.

Especially preferred are compounds of formula I wherein R² and R³ each independently are C₁-C₁₀-alkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, C₃-C₈-cycloalkyl, or phenyl, wherein these groups are unsubstituted or substituted by any combination of 1 to 6 groups selected from R¹⁰ or R¹¹, and

R¹⁰ is C₁-C₁₀-alkyl, C₃-C₈-cycloalkyl, C₁-C₁₀-alkyl-C₃-C₈-cycloalkyl or

a saturated, partially unsaturated or unsaturated 3- to 8-membered ring which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, wherein these groups are unsubstituted or substituted with any combination of from 1 to 6 groups R¹¹, and

R¹¹ is halogen, cyano, nitro, hydroxy, mercapto, amino, formyl, C₁-C₁₀-alkylcarbonyl, C₁-C₁₀-alkoxy, C₂-C₁₀-alkenyloxy, C₂-C₁₀-alkynyloxy, C₁-C₁₀-haloalkoxy, C₃-C₈-cycloalkoxy, C₃-C₈-halocycloalkoxy, C₁-C₁₀-alkoxycarbonyl, C₃-C₈-cycloalkoxycarbonyl, C₁-C₁₀-alkylcarbonyloxy, C₃-C₈-cyclo alkylcarbonyloxy, C₁-C₁₀-haloalkoxycarbonyl, C₁-C₁₀-haloalkylcarbonyloxy, C₁-C₁₀-alkanamido, C₃-C₈-cycloalkanamido, C₁-C₁₀-alkylthio, C₂-C₁₀-alkenylthio, C₂-C₁₀-alkynylthio, C₁-C₁₀-haloalkylthio, C₃-C₈-cycloalkylthio, C₃-C₈-halocycloalkylthio, C₃-C₈-cycloalkyl-C₁-C₄-alkylthio, C₂-C₁₀-alkenylsulfinyl, C₂-C₁₀-alkynylsulfinyl, C₁-C₁₀-haloalkylsulfinyl, C₃-C₈-cycloalkylsulfinyl, C₃-C₈-halocycloalkenylsulfinyl, C₃-C₈-cycloalkyl-C₁-C₄-alkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₂-C₁₀-alkenylsulfonyl, C₂-C₁₀-alkynylsulfonyl, C₁-C₁₀-haloalkylsulfonyl, C₃-C₈-cycloalkylsulfonyl, C₃-C₈-halocycloalkylsulfonyl, C₃-C₈-cycloalkyl-C₁-C₄-alkylsulfonyl, di(C₁-C₁₀-alkyl)amino, C₁-C₁₀-alkylamino, C₂-C₁₀-alkenylamino, C₂-C₁₀-alkynylamino, C₁-C₁₀-alkyl-C₂-C₁₀-alkenylamino, C₁-C₁₀-alkyl-C₂-C₁₀-alkynylamino, C₁-C₁₀-haloalkylamino, C₂-C₁₀-haloalkenylamino, C₃-C₈-cycloalkylamino, tri(C₁-C₁₀-alkyl)silyl, aryl, aryloxy, arylthio, arylamino, wherein aryl is phenyl, naphthyl or biphenyl, or a saturated, partially unsaturated or unsaturated 3- to 8-membered ring system which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, wherein these aryl and these heterocyclic ringsystems are unsubstituted or substituted with any combination of from 1 to 6 groups selected from halogen, cyano, nitro, amino, hydroxy, mercapto, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkylthio, C₁-C₄-haloalkylthio, di(C₁-C₄-alkyl)amino and C₁-C₄-alkylamino.

More preferred are compounds of formula I wherein R² and R³ each independently are C₁-C₁₀alkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, C₃-C₈-cycloalkyl, or phenyl, wherein these groups are unsubstituted or substituted by any combination of 1 to 6 groups selected from R¹¹, and

R¹¹ is halogen, cyano, nitro, hydroxy, mercapto, amino, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₃-C₈-cycloalkoxy, C₁-C₁₀-alkoxycarbonyl, C₁-C₁₀-alkylcarbonyloxy, C₁-C₁₀-alkanamido, C₁-C₁₀-alkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-alkylsulfonyl, di(C₁-C₁₀-alkyl)amino or C₁-C₁₀-alkylamino.

Preferred are also compounds of formula I wherein R² and R³ together with the sulfur atom to which they are attached form a 5- or 6-membered heterocycle which besides the sulfur atom contains 1 nitrogen or 1 oxygen atom, wherein these groups are un-substituted or substituted by any combination of 1 to 6 groups selected from with any combination of from 1 to 6 groups selected from halogen, cyano, nitro, amino, hydroxy, mercapto, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkylthio, C₁-C₄-haloalkylthio, di(C₁-C₄-alkyl)amino and C₁-C₄-alkylamino.

Preferred are also compounds of formula I wherein R² and R³ together with the sulfur atom to which they are attached form a unit SR²R³ of the following formula:

wherein

-   r is 0 or 1; -   D is a direct bond, branched or straight C₁-C₄-alkylene, O,     S(O)_(0,1,2) or NR^(j), preferably CH₂, O, or NR^(j); -   R⁹ is as defined above for compounds of formula I; -   R^(j) is hydrogen, C₁-C₄-alkyl, C₁-C₄-alkylcarbonyl,     C₁-C₄-alkoxycarbonyl, C₁-C₄-alkylaminocarbonyl,     di(C₁-C₄-alkyl)aminocarbonyl, or C₁-C₄-alkylsulfonyl; -   a,b are the same or different 0, 1, 2, 3 or 4, preferably 0, 1, or     2. -   When r=0 then the both arylgroups are unbridged.

Preferred are compounds of formula I wherein R⁹ is R¹⁰, R¹¹, or —C(═O)R¹⁰, —, C(═NOR¹⁰)R¹⁰, —C(═NNR¹⁰ ₂)R¹⁰, —C(═O)OR¹⁰, —C(═O)NR¹⁰ ₂, —C(═O)NR¹⁰—NR¹⁰ ₂, —C(═O)NR¹⁰—NR¹⁰[C(═O)R¹⁰], —SO₂NR¹⁰ ₂, —OR¹⁰, —NR¹⁰ ₂, or —SR¹⁰.

Preferred are compounds of formula I wherein R⁴ is NR¹²R¹³ and

R¹² and R¹³ are each independently hydrogen, C₁-C₂₀-alkyl, C₂-C₂₀-alkenyl or C₂-C₂₀-alkynyl, each of which is unsubstituted or substituted by from 1 to 6 groups selected from C₁-C₄-alkoxy, C₁-C₄-alkylthio, CN, NO₂, formyl, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxycarbonyl, C₁-C₄-alkylaminocarbonyl, di(C₁-C₄-alkyl)aminocarbonyl, C₁-C₄-alkylsulfinyl, C₁-C₄-alkylsulfonyl, C₃-C₈-cycloalkyl, and phenyl, wherein phenyl itself is unsubstituted or substituted by 1 to 4 substituents selected from halogen, C₁-C₄-alkyl, C₁-C₄-alkoxy, C₁-C₄-fluoroalkyl, C₁-C₄-alkyloxycarbonyl, trifluoromethylsulfonyl, formyl, nitro and cyano; or C₁-C₂₀-haloalkyl, C₂-C₂₀-haloalkenyl, C₂-C₂₀-haloalkynyl, C₅-C₁₀-cycloalkenyl, or a saturated or partially unsaturated or unsaturated 3- to 8-membered ring system which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, wherein this ring system is unsubstituted or substituted by 1 to 4 substituents selected from halogen, C₁-C₄-alkyl, C₁-C₄-alkoxy, C₁-C₄-fluoroalkyl, C₁-C₄-alkyloxycarbonyl, trifluoromethylsulfonyl, formyl, nitro and cyano; or R¹² and R¹³ together with the nitrogen atom to which they are attached may also form a saturated or partially unsaturated 5- to 8-membered heterocycle which besides the one nitrogen atom contains 0 to 2 further heteroatoms selected from oxygen, nitrogen, sulfur and may contain 1 or 2 carbonyl groups or thiocarbonyl groups and which is unsubstituted or substituted by from 1 to 4 groups selected from C₁-C₄-alkyl, C₁-C₄-alkoxy and C₁-C₄-haloalkyl.

More preferred are compounds of formula I wherein R⁴ is NR¹²R¹³ and

R¹² and R¹³ are each independently hydrogen, C₁-C₂₀-alkyl, C₂-C₂₀alkenyl or C₂-C₂₀-alkynyl, each of which is unsubstituted or substituted by from 1 to 3 CN, C₁-C₂₀ haloalkyl, or R¹² and R¹³ together with the nitrogen atom to which they are attached may also form a saturated or partially unsaturated 5- to 8-membered heterocycle which besides the one nitrogen atom contains 0 to 2 further heteroatoms selected from oxygen, nitrogen, sulfur, and may contain 1 or 2 carbonyl groups or thiocarbonyl groups and which is unsubstituted or substituted by from 1 to 4 groups selected from C₁-C₄-alkyl, C₁-C₄-alkoxy and C₁-C₄-haloalkyl.

Especially preferred are compounds of formula I wherein R⁴ is NR¹²R¹³ and R¹² and R¹³ together with the nitrogen atom to which they are attached are a saturated or partially unsaturated 5- or 6-membered nitrogen heterocycle which may be substituted by from 1 to 4 groups selected from C₁-C₄-alkyl, C₁-C₄-alkoxy and C₁-C₄-haloalkyl, in particular 2,5-dihydropyrrol-1-yl, 2,3-dihydropyrrol-1-yl, 1-pyrrolidinyl, 1-piperidinyl, 4-morpholinyl, 2-methylmorpholin-4-yl, 2,6-dimethylmorpholin-4-yl, or 1-methylpiperazin-4-yl.

Preferred are compounds of formula I wherein R⁵ is hydrogen.

Preferred are compounds of formula I wherein Q¹ is hydrogen, halogen, cyano, SCN, nitro, hydroxy, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₃-C₈-cycloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-alkylsulfonyloxy, C₁-C₁₀-alkylamino or di(C₁-C₁₀-alkyl)amino, most preferably hydrogen, halogen, cyano, C₁-C₄-alkyl or C₁-C₄-haloalkyl.

Preferred are compounds of formula I wherein Q² is halogen, cyano, SCN, nitro, hydroxy, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₃-C₈-cycloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-alkylsulfonyloxy, C₁-C₁₀-alkylamino or di(C₁-C₁₀-alkyl)amino, most preferably halogen, cyano, C₁-C₄-alkyl or C₁-C₄-haloalkyl.

Preferred are compounds of formula I wherein Q³ is halogen, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkynyl, C₃-C₀₈-cycloalkyl, C₃-C₈-halocycloalkyl, each unsubstituted or independently substituted with 1 to 2 groups selected from cyano, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy or C₁-C₁₀-alkylthio, or

Q³ is OR¹⁴, S(O)_(q)R¹⁴, NR¹⁵R¹⁶, OS(O)₂R¹⁷, C(S)NH₂, C(R¹⁸)═NOR¹⁸; and

R¹⁴ is C₁-C₁₀-alkyl or C₃-C₈-cycloalkyl unsubstituted or substituted with 1 R¹⁹; and

R¹⁵ is C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, each unsubstituted or substituted with 1 R¹⁹; and

R¹⁶ is hydrogen, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, each unsubstituted or substituted with 1 R¹⁹; and

R¹⁷ is C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, C₃-C₈-cycloalkyl, each unsubstituted or substituted with 1 R¹⁹; and

R¹⁸ is hydrogen, C₁-C₁₀-alkyl, or C₁-C₁₀-haloalkyl; and

R¹⁹ is cyano, nitro, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, or C₁-C₁₀-haloalkylthio.

Most preferred are compounds of formula I wherein Q³ is halogen, C₁-C₄-haloalkyl or C₁-C₄-haloalkoxy.

Preferred are compounds of formula I wherein Q⁴ is halogen, cyano, nitro, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-haloalkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-haloalkylsulfonyl, or C₁-C₁₀-alkoxycarbonyl, preferably halogen or C₁-C₄-haloalkyl.

Preferred are compounds of formula I wherein X and Y are oxygen.

Preferred are compounds of formula I wherein W is N or CQ⁴, preferably N.

Preferred are compounds of formula I wherein m is 2.

Preferred are compounds of formula I wherein n is 0.

Preferred are compounds of formula I wherein V and V′ each independently are N or CH. Preferably, both V and V′ are CH.

Especially preferred are N-thio-anthranilamid compounds of formula I wherein

W is N

R¹ is hydrogen;

Q¹ is hydrogen, halogen, cyano, C₁-C₄-alkyl or C₁-C₄-haloalkyl;

Q² is halogen, cyano, C₁-C₄-alkyl or C₁-C₄-haloalkyl;

Q³ is halogen, C₁-C₄-haloalkyl or C₁-C₄-haloalkoxy;

Q⁴ is halogen or C₁-C₄-haloalkyl and is in the ortho-position; and

p is 1.

Also, especially preferred are N-thio-anthranilamid compounds of formula I wherein

-   A is A²; -   R⁴ is C₁-C₆-alkylamino, C₂-C₆-alkenylamino, C₂-C₆-alkynylamino,     di(C₁-C₆-alkyl)amino, di(C₂-C₆-alkenyl)amino,     di(C₂-C₆-alkynyl)amino, (phenyl)(C₁-C₆-alkyl)amino,     (phenyl)(C₂-C₆-alkenyl)amino, (phenyl)(C₂-C₆-alkynyl)amino,     piperidine, piperazin or morpholine; and -   R⁵ is hydrogen or C₁-C₄-alkyl.

Also, especially preferred are N-thio-anthranilamid compounds of formula I wherein

-   A is A¹; and -   R² and R³ each independently are phenyl, C₁-C₆-alkyl, C₂-C₆-alkenyl,     or C₂-C₆-alkynyl, which are unsubstituted or substituted with any     combination of 1 to 6 groups selected from halogen and cyano.

Most preferred are compounds of formula I wherein R² and R³ each independently are C₁-C₄-alkyl, phenylmethyl, allylmethyl, propargylmethyl, or together with the sulfur atom to which they are attached form a 3- to 6-membered saturated ring which contains 1 to 3 heteroatoms selected from sulfur and oxygen.

With respect to their use, particular preference is given to the compounds IA compiled in the tables below. Moreover, the groups mentioned for a substituent in the tables are on their own, independently of the combination in which they are mentioned, a particularly preferred embodiment of the substituent in question.

Table 1

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CF₃, and A in each case corresponds to a row of Table A.

Table 2

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes bromine, and A in each case corresponds to a row of Table A.

Table 3

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes chlorine, and A in each case corresponds to a row of Table A.

Table 4

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₃, and A in each case corresponds to a row of Table A.

Table 5

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₃, and A in each case corresponds to a row of Table A.

Table 6

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCHCH₂, and A in each case corresponds to a row of Table A.

Table 7

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes ethoxy, and A in each case corresponds to a row of Table A.

Table 8

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a row of Table A.

Table 9

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂CH═CH₂, and A in each case corresponds to a row of Table A.

Table 10

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂CCH, and A in each case corresponds to a row of Table A.

Table 11

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂OCH₃, and A in each case corresponds to a row of Table A.

Table 12

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 13

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂SCH₃, and A in each case corresponds to a row of Table A.

Table 14

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 15

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂S(═O)CH₃, and A in each case corresponds to a row of Table A.

Table 16

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a row of Table A.

Table 17

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a row of Table A.

Table 18

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table A.

Table 19

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a row of Table A.

Table 20

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table A.

Table 21

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a row of Table A.

Table 22

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a row of Table A.

Table 23

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OC(═O)CF₃, and A in each case corresponds to a row of Table A.

Table 24

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes NHCH₂CF₃, and A in each case corresponds to a row of Table A.

Table 25

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a row of Table A.

Table 26

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a row of Table A.

Table 27

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a row of Table A.

Table 28

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a row of Table A.

Table 29

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a row of Table A.

Table 30

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂CN, and A in each case corresponds to a row of Table A.

Table 31

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂NO₂, and A in each case corresponds to a row of Table A.

Table 32

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes cyclopropyloxy, and A in each case corresponds to a row of Table A.

Table 33

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a row of Table A.

Table 34

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a row of Table A.

Table 35

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH═NOCH₃, and A in each case corresponds to a row of Table A.

Table 36

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH═NOCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 37

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a row of Table A.

Table 38

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a row of Table A.

Table 39

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a row of Table A.

Table 40

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 41

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a row of Table A.

Table 42

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a row of Table A.

Table 43

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CF₃, and A in each case corresponds to a row of Table A.

Table 44

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes bromine, and A in each case corresponds to a row of Table A.

Table 45

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes chlorine, and A in each case corresponds to a row of Table A.

Table 46

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₃, and A in each case corresponds to a row of Table A.

Table 47

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₃, and A in each case corresponds to a row of Table A.

Table 48

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCHCH₂, and A in each case corresponds to a row of Table A.

Table 49

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes ethoxy, and A in each case corresponds to a row of Table A.

Table 50

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a row of Table A.

Table 51

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂CH═CH₂, and A in each case corresponds to a row of Table A.

Table 52

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂CCH, and A in each case corresponds to a row of Table A.

Table 53

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂OCH₃, and A in each case corresponds to a row of Table A.

Table 54

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 55

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂SCH₃, and A in each case corresponds to a row of Table A.

Table 56

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 57

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂S(═O)CH₃, and A in each case corresponds to a row of Table A.

Table 58

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a row of Table A.

Table 59

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a row of Table A.

Table 60

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table A.

Table 61

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a row of Table A.

Table 62

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table A.

Table 63

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a row of Table A.

Table 64

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a row of Table A.

Table 65

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OC(═O)CF₃, and A in each case corresponds to a row of Table A.

Table 66

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes NHCH₂CF₃, and A in each case corresponds to a row of Table A.

Table 67

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a row of Table A.

Table 68

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a row of Table A.

Table 69

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a row of Table A.

Table 70

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a row of Table A.

Table 71

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a row of Table A.

Table 72

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂CN, and A in each case corresponds to a row of Table A.

Table 73

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂NO₂, and A in each case corresponds to a row of Table A.

Table 74

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes cyclopropyloxy, and A in each case corresponds to a row of Table A.

Table 75

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a row of Table A.

Table 76

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a row of Table A.

Table 77

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH═NOCH₃, and A in each case corresponds to a row of Table A.

Table 78

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH═NOCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 79

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a row of Table A.

Table 80

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a row of Table A.

Table 81

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a row of Table A.

Table 82

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 83

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a row of Table A.

Table 84

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a row of Table A.

Table 85

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CF₃, and A in each case corresponds to a row of Table A.

Table 86

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes bromine, and A in each case corresponds to a row of Table A.

Table 87

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes chlorine, and A in each case corresponds to a row of Table A.

Table 88

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₃, and A in each case corresponds to a row of Table A.

Table 89

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₃, and A in each case corresponds to a row of Table A.

Table 90

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCHCH₂, and A in each case corresponds to a row of Table A.

Table 91

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes ethoxy, and A in each case corresponds to a row of Table A.

Table 92

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a row of Table A.

Table 93

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂CH═CH₂, and A in each case corresponds to a row of Table A.

Table 94

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂CCH, and A in each case corresponds to a row of Table A.

Table 95

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂OCH₃, and A in each case corresponds to a row of Table A.

Table 96

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 97

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂SCH₃, and A in each case corresponds to a row of Table A.

Table 98

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 99

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂S(═O)CH₃, and A in each case corresponds to a row of Table A.

Table 100

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a row of Table A.

Table 101

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a row of Table A.

Table 102

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table A.

Table 103

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a row of Table A.

Table 104

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table A.

Table 105

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a row of Table A.

Table 106

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a row of Table A.

Table 107

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OC(═O)CF₃, and A in each case corresponds to a row of Table A.

Table 108

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes NHCH₂CF₃, and A in each case corresponds to a row of Table A.

Table 109

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a row of Table A.

Table 110

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a row of Table A.

Table 111

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a row of Table A.

Table 112

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a row of Table A.

Table 113

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a row of Table A.

Table 114

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂CN, and A in each case corresponds to a row of Table A.

Table 115

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂NO₂, and A in each case corresponds to a row of Table A.

Table 116

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes cyclopropyloxy, and A in each case corresponds to a row of Table A.

Table 117

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a row of Table A.

Table 118

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a row of Table A.

Table 119

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH═NOCH₃, and A in each case corresponds to a row of Table A.

Table 120

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH═NOCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 121

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a row of Table A.

Table 122

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a row of Table A.

Table 123

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a row of Table A.

Table 124

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 125

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a row of Table A.

Table 126

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a row of Table A.

Table 127

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CF₃, and A in each case corresponds to a row of Table A.

Table 128

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes bromine, and A in each case corresponds to a row of Table A.

Table 129

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes chlorine, and A in each case corresponds to a row of Table A.

Table 130

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₃, and A in each case corresponds to a row of Table A.

Table 131

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₃, and A in each case corresponds to a row of Table A.

Table 132

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCHCH₂, and A in each case corresponds to a row of Table A.

Table 133

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes ethoxy, and A in each case corresponds to a row of Table A.

Table 134

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a row of Table A.

Table 135

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂CH═CH₂, and A in each case corresponds to a row of Table A.

Table 136

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂CCH, and A in each case corresponds to a row of Table A.

Table 137

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂OCH₃, and A in each case corresponds to a row of Table A.

Table 138

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 139

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂SCH₃, and A in each case corresponds to a row of Table A.

Table 140

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 141

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂S(═O)CH₃, and A in each case corresponds to a row of Table A.

Table 142

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a row of Table A.

Table 143

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a row of Table A.

Table 144

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table A.

Table 145

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a row of Table A.

Table 146

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table A.

Table 147

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a row of Table A.

Table 148

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a row of Table A.

Table 149

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OC(═O)CF₃, and A in each case corresponds to a row of Table A.

Table 150

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes NHCH₂CF₃, and A in each case corresponds to a row of Table A.

Table 151

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a row of Table A.

Table 152

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a row of Table A.

Table 153

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a row of Table A.

Table 154

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a row of Table A.

Table 155

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a row of Table A.

Table 156

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂CN, and A in each case corresponds to a row of Table A.

Table 157

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂NO₂, and A in each case corresponds to a row of Table A.

Table 158

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes cyclopropyloxy, and A in each case corresponds to a row of Table A.

Table 159

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a row of Table A.

Table 160

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a row of Table A.

Table 161

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH═NOCH₃, and A in each case corresponds to a row of Table A.

Table 162

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH═NOCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 163

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a row of Table A.

Table 164

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a row of Table A.

Table 165

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a row of Table A.

Table 166

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 167

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a row of Table A.

Table 168

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a row of Table A.

Table 169

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CF₃, and A in each case corresponds to a row of Table A.

Table 170

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes bromine, and A in each case corresponds to a row of Table A.

Table 171

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes chlorine, and A in each case corresponds to a row of Table A.

Table 172

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₃, and A in each case corresponds to a row of Table A.

Table 173

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₃, and A in each case corresponds to a row of Table A.

Table 174

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCHCH₂, and A in each case corresponds to a row of Table A.

Table 175

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes ethoxy, and A in each case corresponds to a row of Table A.

Table 176

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a row of Table A.

Table 177

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂CH═CH₂, and A in each case corresponds to a row of Table A.

Table 178

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂CCH, and A in each case corresponds to a row of Table A.

Table 179

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂OCH₃, and A in each case corresponds to a row of Table A.

Table 180

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 181

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂SCH₃, and A in each case corresponds to a row of Table A

Table 182

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 183

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂S(═O)CH₃, and A in each case corresponds to a row of Table A.

Table 184

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a row of Table A.

Table 185

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a row of Table A.

Table 186

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table A.

Table 187

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a row of Table A.

Table 188

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table A.

Table 189

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a row of Table A.

Table 190

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a row of Table A.

Table 191

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OC(═O)CF₃, and A in each case corresponds to a row of Table A.

Table 192

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes NHCH₂CF₃, and A in each case corresponds to a row of Table A.

Table 193

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a row of Table A.

Table 194

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a row of Table A.

Table 195

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a row of Table A.

Table 196

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a row of Table A.

Table 197

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a row of Table A.

Table 198

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂CN, and A in each case corresponds to a row of Table A.

Table 199

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂NO₂, and A in each case corresponds to a row of Table A.

Table 200

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes cyclopropyloxy, and A in each case corresponds to a row of Table A.

Table 201

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a row of Table A.

Table 202

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a row of Table A.

Table 203

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH═NOCH₃, and A in each case corresponds to a row of Table A.

Table 204

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH═NOCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 205

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a row of Table A.

Table 206

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a row of Table A.

Table 207

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a row of Table A.

Table 208

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 209

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a row of Table A.

Table 210

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a row of Table A.

Table 211

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CF₃, and A in each case corresponds to a row of Table A.

Table 212

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes bromine, and A in each case corresponds to a row of Table A.

Table 213

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes chlorine, and A in each case corresponds to a row of Table A.

Table 214

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₃, and A in each case corresponds to a row of Table A.

Table 215

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₃, and A in each case corresponds to a row of Table A.

Table 216

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCHCH₂, and A in each case corresponds to a row of Table A.

Table 217

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes ethoxy, and A in each case corresponds to a row of Table A.

Table 218

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a row of Table A.

Table 219

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂CH═CH₂, and A in each case corresponds to a row of Table A.

Table 220

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂CCH, and A in each case corresponds to a row of Table A.

Table 221

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂OCH₃, and A in each case corresponds to a row of Table A.

Table 222

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 223

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂SCH₃, and A in each case corresponds to a row of Table A.

Table 224

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 225

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂S(═O)CH₃, and A in each case corresponds to a row of Table A.

Table 226

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a row of Table A.

Table 227

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a row of Table A.

Table 228

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table A.

Table 229

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a row of Table A.

Table 230

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table A.

Table 231

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a row of Table A.

Table 232

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a row of Table A.

Table 233

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OC(═O)CF₃, and A in each case corresponds to a row of Table A.

Table 234

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes NHCH₂CF₃, and A in each case corresponds to a row of Table A.

Table 235

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a row of Table A.

Table 236

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a row of Table A.

Table 237

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a row of Table A.

Table 238

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a row of Table A.

Table 239

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a row of Table A.

Table 240

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂CN, and A in each case corresponds to a row of Table A.

Table 241

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂NO₂, and A in each case corresponds to a row of Table A.

Table 242

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes cyclopropyloxy, and A in each case corresponds to a row of Table A.

Table 243

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a row of Table A.

Table 244

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a row of Table A.

Table 245

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH═NOCH₃, and A in each case corresponds to a row of Table A.

Table 246

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH═NOCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 247

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a row of Table A.

Table 248

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a row of Table A.

Table 249

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a row of Table A.

Table 250

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 251

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a row of Table A.

Table 252

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a row of Table A.

Table 253

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CF₃, and A in each case corresponds to a row of Table A.

Table 254

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes bromine, and A in each case corresponds to a row of Table A.

Table 255

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes chlorine, and A in each case corresponds to a row of Table A.

Table 256

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₃, and A in each case corresponds to a row of Table A.

Table 257

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₃, and A in each case corresponds to a row of Table A.

Table 258

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCHCH₂, and A in each case corresponds to a row of Table A.

Table 259

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes ethoxy, and A in each case corresponds to a row of Table A.

Table 260

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a row of Table A.

Table 261

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂CH═CH₂, and A in each case corresponds to a row of Table A.

Table 262

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂CCH, and A in each case corresponds to a row of Table A.

Table 263

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂OCH₃, and A in each case corresponds to a row of Table A.

Table 264

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 265

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂SCH₃, and A in each case corresponds to a row of Table A.

Table 266

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 267

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂S(═O)CH₃, and A in each case corresponds to a row of Table A.

Table 268

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a row of Table A.

Table 269

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a row of Table A.

Table 270

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table A.

Table 271

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a row of Table A.

Table 272

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table A.

Table 273

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a row of Table A.

Table 274

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a row of Table A.

Table 275

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OC(═O)CF₃, and A in each case corresponds to a row of Table A.

Table 276

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes NHCH₂CF₃, and A in each case corresponds to a row of Table A.

Table 277

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a row of Table A.

Table 278

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a row of Table A.

Table 279

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a row of Table A.

Table 280

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a row of Table A.

Table 281

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a row of Table A.

Table 282

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂CN, and A in each case corresponds to a row of Table A.

Table 283

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂NO₂, and A in each case corresponds to a row of Table A.

Table 284

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes cyclopropyloxy, and A in each case corresponds to a row of Table A.

Table 285

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a row of Table A.

Table 286

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a row of Table A.

Table 287

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH═NOCH₃, and A in each case corresponds to a row of Table A.

Table 288

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH═NOCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 289

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a row of Table A.

Table 290

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a row of Table A.

Table 291

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a row of Table A.

Table 292

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a row of Table A.

Table 293

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a row of Table A.

Table 294

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a row of Table A.

TABLE A No. A R^(a) R^(b) R^(c) IA-1

H CH₃ CH₃ IA-2 A².1 H CH₂CH₃ CH₃ IA-3 A².1 H CH₂CH₂CH₃ CH₃ IA-4 A².1 H CH(CH₃)₂ CH₃ IA-5 A².1 H CH₂CH₂CH₂CH₃ CH₃ IA-6 A².1 H CH₂CH(CH₃)₂ CH₃ IA-7 A².1 H CH₂CHCH₂ CH₃ IA-8 A².1 H CH₂CCH CH₃ IA-9 A².1 H C₆H₅ CH₃ IA-10 A².1 CH₃ CH₃ CH₃ IA-11 A².1 CH₃ CH₂CH₃ CH₃ IA-12 A².1 CH₃ CH₂CH₂CH₃ CH₃ IA-13 A².1 CH₃ CH(CH₃)₂ CH₃ IA-14 A².1 CH₃ CH₂CH₂CH₂CH₃ CH₃ IA-15 A².1 CH₃ CH₂CH(CH₃)₂ CH₃ IA-16 A².1 CH₃ CH₂CHCH₂ CH₃ IA-17 A².1 CH₃ CH₂CCH CH₃ IA-18 A².1 CH₃ C₆H₅ CH₃ IA-19 A².1 CH(CH₃)₂ CH₃ CH₃ IA-20 A².1 CH(CH₃)₂ CH₂CH₃ CH₃ IA-21 A².1 CH(CH₃)₂ CH₂CH₂CH₃ CH₃ IA-22 A².1 CH(CH₃)₂ CH(CH₃)₂ CH₃ IA-23 A².1 CH(CH₃)₂ CH₂CH₂CH₂CH₃ CH₃ IA-24 A².1 CH(CH₃)₂ CH₂CH(CH₃)₂ CH₃ IA-25 A².1 CH(CH₃)₂ CH₂CHCH₂ CH₃ IA-26 A².1 CH(CH₃)₂ CH₂CCH CH₃ IA-27 A².1 CH(CH₃)₂ C₆H₅ CH₃ IA-28 A².1 H CH₂CH₃ CH₂CH₃ IA-29 A².1 H CH₂CH₂CH₃ CH₂CH₃ IA-30 A².1 H CH(CH₃)₂ CH₂CH₃ IA-31 A².1 H CH₂CH₂CH₂CH₃ CH₂CH₃ IA-32 A².1 H CH₂CH(CH₃)₂ CH₂CH₃ IA-33 A².1 H CH₂CHCH₂ CH₂CH₃ IA-34 A².1 H CH₂CCH CH₂CH₃ IA-35 A².1 H C₆H₅ CH₂CH₃ IA-36 A².1 CH₃ CH₂CH₃ CH₂CH₃ IA-37 A².1 CH₃ CH₂CH₂CH₃ CH₂CH₃ IA-38 A².1 CH₃ CH(CH₃)₂ CH₂CH₃ IA-39 A².1 CH₃ CH₂CH₂CH₂CH₃ CH₂CH₃ IA-40 A².1 CH₃ CH₂CH(CH₃)₂ CH₂CH₃ IA-41 A².1 CH₃ CH₂CHCH₂ CH₂CH₃ IA-42 A².1 CH₃ CH₂CCH CH₂CH₃ IA-43 A².1 CH₃ C₆H₅ CH₂CH₃ IA-44 A².1 CH(CH₃)₂ CH₂CH₃ CH₂CH₃ IA-45 A².1 CH(CH₃)₂ CH₂CH₂CH₃ CH₂CH₃ IA-46 A².1 CH(CH₃)₂ CH(CH₃)₂ CH₂CH₃ IA-47 A².1 CH(CH₃)₂ CH₂CH₂CH₂CH₃ CH₂CH₃ IA-48 A².1 CH(CH₃)₂ CH₂CH(CH₃)₂ CH₂CH₃ IA-49 A².1 CH(CH₃)₂ CH₂CHCH₂ CH₂CH₃ IA-50 A².1 CH(CH₃)₂ CH₂CCH CH₂CH₃ IA-51 A².1 CH(CH₃)₂ C₆H₅ CH₂CH₃ IA-52 A².1 H CH₂CH₂CH₃ CH₂CH₂CH₃ IA-53 A².1 H CH(CH₃)₂ CH₂CH₂CH₃ IA-54 A².1 H CH₂CH₂CH₂CH₃ CH₂CH₂CH₃ IA-55 A².1 H CH₂CH(CH₃)₂ CH₂CH₂CH₃ IA-56 A².1 H CH₂CHCH₂ CH₂CH₂CH₃ IA-57 A².1 H CH₂CCH CH₂CH₂CH₃ IA-58 A².1 H C₆H₅ CH₂CH₂CH₃ IA-59 A².1 CH₃ CH₂CH₂CH₃ CH₂CH₂CH₃ IA-60 A².1 CH₃ CH(CH₃)₂ CH₂CH₂CH₃ IA-61 A².1 CH₃ CH₂CH₂CH₂CH₃ CH₂CH₂CH₃ IA-62 A².1 CH₃ CH₂CH(CH₃)₂ CH₂CH₂CH₃ IA-63 A².1 CH₃ CH₂CHCH₂ CH₂CH₂CH₃ IA-64 A².1 CH₃ CH₂CCH CH₂CH₂CH₃ IA-65 A².1 CH₃ C₆H₅ CH₂CH₂CH₃ IA-66 A².1 CH(CH₃)₂ CH₂CH₂CH₃ CH₂CH₂CH₃ IA-67 A².1 CH(CH₃)₂ CH(CH₃)₂ CH₂CH₂CH₃ IA-68 A².1 CH(CH₃)₂ CH₂CH₂CH₂CH₃ CH₂CH₂CH₃ IA-69 A².1 CH(CH₃)₂ CH₂CH(CH₃)₂ CH₂CH₂CH₃ IA-70 A².1 CH(CH₃)₂ CH₂CHCH₂ CH₂CH₂CH₃ IA-71 A².1 CH(CH₃)₂ CH₂CCH CH₂CH₂CH₃ IA-72 A².1 CH(CH₃)₂ C₆H₅ CH₂CH₂CH₃ IA-73 A².1 H CH(CH₃)₂ CH(CH₃)₂ IA-74 A².1 H CH₂CH₂CH₂CH₃ CH(CH₃)₂ IA-75 A².1 H CH₂CH(CH₃)₂ CH(CH₃)₂ IA-76 A².1 H CH₂CHCH₂ CH(CH₃)₂ IA-77 A².1 H CH₂CCH CH(CH₃)₂ IA-78 A².1 H C₆H₅ CH(CH₃)₂ IA-79 A².1 CH₃ CH(CH₃)₂ CH(CH₃)₂ IA-80 A².1 CH₃ CH₂CH₂CH₂CH₃ CH(CH₃)₂ IA-81 A².1 CH₃ CH₂CH(CH₃)₂ CH(CH₃)₂ IA-82 A².1 CH₃ CH₂CHCH₂ CH(CH₃)₂ IA-83 A².1 CH₃ CH₂CCH CH(CH₃)₂ IA-84 A².1 CH₃ C₆H₅ CH(CH₃)₂ IA-85 A².1 CH(CH₃)₂ CH(CH₃)₂ CH(CH₃)₂ IA-86 A².1 CH(CH₃)₂ CH₂CH₂CH₂CH₃ CH(CH₃)₂ IA-87 A².1 CH(CH₃)₂ CH₂CH(CH₃)₂ CH(CH₃)₂ IA-88 A².1 CH(CH₃)₂ CH₂CHCH₂ CH(CH₃)₂ IA-89 A².1 CH(CH₃)₂ CH₂CCH CH(CH₃)₂ IA-90 A².1 CH(CH₃)₂ C₆H₅ CH(CH₃)₂ IA-91 A².1 H CH₂CH₂CH₂CH₃ CH₂CH₂CH₂CH₃ IA-92 A².1 H CH₂CH(CH₃)₂ CH₂CH₂CH₂CH₃ IA-93 A².1 H CH₂CHCH₂ CH₂CH₂CH₂CH₃ IA-94 A².1 H CH₂CCH CH₂CH₂CH₂CH₃ IA-95 A².1 H C₆H₅ CH₂CH₂CH₂CH₃ IA-96 A².1 CH₃ CH₂CH₂CH₂CH₃ CH₂CH₂CH₂CH₃ IA-97 A².1 CH₃ CH₂CH(CH₃)₂ CH₂CH₂CH₂CH₃ IA-98 A².1 CH₃ CH₂CHCH₂ CH₂CH₂CH₂CH₃ IA-99 A².1 CH₃ CH₂CCH CH₂CH₂CH₂CH₃ IA-100 A².1 CH₃ C₆H₅ CH₂CH₂CH₂CH₃ IA-101 A².1 CH(CH₃)₂ CH₂CH₂CH₂CH₃ CH₂CH₂CH₂CH₃ IA-102 A².1 CH(CH₃)₂ CH₂CH(CH₃)₂ CH₂CH₂CH₂CH₃ IA-103 A².1 CH(CH₃)₂ CH₂CHCH₂ CH₂CH₂CH₂CH₃ IA-104 A².1 CH(CH₃)₂ CH₂CCH CH₂CH₂CH₂CH₃ IA-105 A².1 CH(CH₃)₂ C₆H₅ CH₂CH₂CH₂CH₃ IA-106 A².1 H CH₂CH(CH₃)₂ CH₂CH(CH₃)₂ IA-107 A².1 H CH₂CHCH₂ CH₂CH(CH₃)₂ IA-108 A².1 H CH₂CCH CH₂CH(CH₃)₂ IA-109 A².1 H C₆H₅ CH₂CH(CH₃)₂ IA-110 A².1 CH₃ CH₂CH(CH₃)₂ CH₂CH(CH₃)₂ IA-111 A².1 CH₃ CH₂CHCH₂ CH₂CH(CH₃)₂ IA-112 A².1 CH₃ CH₂CCH CH₂CH(CH₃)₂ IA-113 A².1 CH₃ C₆H₅ CH₂CH(CH₃)₂ IA-114 A².1 CH(CH₃)₂ CH₂CH(CH₃)₂ CH₂CH(CH₃)₂ IA-115 A².1 CH(CH₃)₂ CH₂CHCH₂ CH₂CH(CH₃)₂ IA-116 A².1 CH(CH₃)₂ CH₂CCH CH₂CH(CH₃)₂ IA-117 A².1 CH(CH₃)₂ C₆H₅ CH₂CH(CH₃)₂ IA-118 A².1 H CH₂CHCH₂ CH₂CHCH₂ IA-119 A².1 H CH₂CCH CH₂CHCH₂ IA-120 A².1 H C₆H₅ CH₂CHCH₂ IA-121 A².1 CH₃ CH₂CHCH₂ CH₂CHCH₂ IA-122 A².1 CH₃ CH₂CCH CH₂CHCH₂ IA-123 A².1 CH₃ C₆H₅ CH₂CHCH₂ IA-124 A².1 CH(CH₃)₂ CH₂CHCH₂ CH₂CHCH₂ IA-125 A².1 CH(CH₃)₂ CH₂CCH CH₂CHCH₂ IA-126 A².1 CH(CH₃)₂ C₆H₅ CH₂CHCH₂ IA-127 A².1 H CH₂CCH CH₂CCH IA-128 A².1 H C₆H₅ CH₂CCH IA-129 A².1 CH₃ CH₂CCH CH₂CCH IA-130 A².1 CH₃ C₆H₅ CH₂CCH IA-131 A².1 CH(CH₃)₂ CH₂CCH CH₂CCH IA-132 A².1 CH(CH₃)₂ C₆H₅ CH₂CCH IA-133 A².1 H C₆H₅ C₆H₅ IA-134 A².1 CH₃ C₆H₅ C₆H₅ IA-135 A².1 CH(CH₃)₂ C₆H₅ C₆H₅ Table 295

Compounds of the formula IA (as defined above) wherein Q¹ denotes hydrogen, Q³ denotes CF₃, and A in each case corresponds to a row of Table B.

Table 296

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes bromine, and A in each case corresponds to a row of Table B.

Table 297

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes chlorine, and A in each case corresponds to a row of Table B.

Table 298

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₃, and A in each case corresponds to a row of Table B.

Table 299

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₃, and A in each case corresponds to a row of Table B.

Table 300

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCHCH₂, and A in each case corresponds to a row of Table B.

Table 301

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes ethoxy, and A in each case corresponds to a row of Table B.

Table 302

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a row of Table B.

Table 303

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂CH═CH₂, and A in each case corresponds to a row of Table B.

Table 304

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂CCH, and A in each case corresponds to a row of Table B.

Table 305

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂OCH₃, and A in each case corresponds to a row of Table B.

Table 306

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a row of Table B.

Table 307

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂SCH₃, and A in each case corresponds to a row of Table B.

Table 308

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a row of Table B.

Table 309

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂S(═O)CH₃, and A in each case corresponds to a row of Table B.

Table 310

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a row of Table B.

Table 311

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a row of Table B.

Table 312

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table B.

Table 313

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a row of Table B.

Table 314

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table B.

Table 315

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a row of Table B.

Table 316

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a row of Table B.

Table 317

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OC(═O)CF₃, and A in each case corresponds to a row of Table B.

Table 318

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes NHCH₂CF₃, and A in each case corresponds to a row of Table B.

Table 319

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a row of Table B.

Table 320

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a row of Table B.

Table 321

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a row of Table B.

Table 322

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a row of Table B.

Table 323

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a row of Table B.

Table 324

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂CN, and A in each case corresponds to a row of Table B.

Table 325

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂NO₂, and A in each case corresponds to a row of Table B.

Table 326

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes cyclopropyloxy, and A in each case corresponds to a row of Table B.

Table 327

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a row of Table B.

Table 328

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a row of Table B.

Table 329

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH═NOCH₃, and A in each case corresponds to a row of Table B.

Table 330

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH═NOCH₂CH₃, and A in each case corresponds to a row of Table B.

Table 331

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a row of Table B.

Table 332

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a row of Table B.

Table 333

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a row of Table B.

Table 334

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a row of Table B.

Table 335

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a row of Table B.

Table 336

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a row of Table B.

Table 337

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CF₃, and A in each case corresponds to a row of Table B.

Table 338

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes bromine, and A in each case corresponds to a row of Table B.

Table 339

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes chlorine, and A in each case corresponds to a row of Table B.

Table 340

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₃, and A in each case corresponds to a row of Table B.

Table 341

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₃, and A in each case corresponds to a row of Table B.

Table 342

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCHCH₂, and A in each case corresponds to a row of Table B.

Table 343

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes ethoxy, and A in each case corresponds to a row of Table B.

Table 344

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a row of Table B.

Table 345

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂CH═CH₂, and A in each case corresponds to a row of Table B.

Table 346

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂CCH, and A in each case corresponds to a row of Table B.

Table 347

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂OCH₃, and A in each case corresponds to a row of Table B.

Table 348

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a row of Table B.

Table 349

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂SCH₃, and A in each case corresponds to a row of Table B.

Table 350

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a row of Table B.

Table 351

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂S(═O)CH₃, and A in each case corresponds to a row of Table B.

Table 352

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a row of Table B.

Table 353

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a row of Table B.

Table 354

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table B.

Table 355

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a row of Table B.

Table 356

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table B.

Table 357

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a row of Table B.

Table 358

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a row of Table B.

Table 359

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OC(═O)CF₃, and A in each case corresponds to a row of Table B.

Table 360

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes NHCH₂CF₃, and A in each case corresponds to a row of Table B.

Table 361

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a row of Table B.

Table 362

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a row of Table B.

Table 363

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a row of Table B.

Table 364

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a row of Table B.

Table 365

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a row of Table B.

Table 366

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂CN, and A in each case corresponds to a row of Table B.

Table 367

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂NO₂, and A in each case corresponds to a row of Table B.

Table 368

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes cyclopropyloxy, and A in each case corresponds to a row of Table B.

Table 369

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a row of Table B.

Table 370

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a row of Table B.

Table 371

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH═NOCH₃, and A in each case corresponds to a row of Table B.

Table 372

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH═NOCH₂CH₃, and A in each case corresponds to a row of Table B.

Table 373

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a row of Table B.

Table 374

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a row of Table B.

Table 375

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a row of Table B.

Table 376

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a row of Table B.

Table 377

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a row of Table B.

Table 378

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a row of Table B.

Table 379

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CF₃, and A in each case corresponds to a row of Table B.

Table 380

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes bromine, and A in each case corresponds to a row of Table B.

Table 381

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes chlorine, and A in each case corresponds to a row of Table B.

Table 382

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₃, and A in each case corresponds to a row of Table B.

Table 383

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₃, and A in each case corresponds to a row of Table B.

Table 384

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCHCH₂, and A in each case corresponds to a row of Table B.

Table 385

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes ethoxy, and A in each case corresponds to a row of Table B.

Table 386

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a row of Table B.

Table 387

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂CH═CH₂, and A in each case corresponds to a row of Table B.

Table 388

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂CCH, and A in each case corresponds to a row of Table B.

Table 389

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂OCH₃, and A in each case corresponds to a row of Table B.

Table 390

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a row of Table B.

Table 391

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂SCH₃, and A in each case corresponds to a row of Table B.

Table 392

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a row of Table B.

Table 393

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂S(═O)CH₃, and A in each case corresponds to a row of Table B.

Table 394

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a row of Table B.

Table 395

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a row of Table B.

Table 396

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table B.

Table 397

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a row of Table B.

Table 398

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table B.

Table 399

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a row of Table B.

Table 400

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a row of Table B.

Table 401

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OC(═O)CF₃, and A in each case corresponds to a row of Table B.

Table 402

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes NHCH₂CF₃, and A in each case corresponds to a row of Table B.

Table 403

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a row of Table B.

Table 404

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a row of Table B.

Table 405

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a row of Table B.

Table 406

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a row of Table B.

Table 407

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a row of Table B.

Table 408

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂CN, and

A in each case corresponds to a row of Table B.

Table 409

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂NO₂, and

A in each case corresponds to a row of Table B.

Table 410

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes cyclopropyloxy, and A in each case corresponds to a row of Table B.

Table 411

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a row of Table B.

Table 412

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a row of Table B.

Table 413

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH═NOCH₃, and A in each case corresponds to a row of Table B.

Table 414

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH═NOCH₂CH₃, and A in each case corresponds to a row of Table B.

Table 415

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a row of Table B.

Table 416

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a row of Table B.

Table 417

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a row of Table B.

Table 418

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a row of Table B.

Table 419

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a row of Table B.

Table 420

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a row of Table B.

Table 421

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CF₃, and A in each case corresponds to a row of Table B.

Table 422

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes bromine, and A in each case corresponds to a row of Table B.

Table 423

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes chlorine, and A in each case corresponds to a row of Table B.

Table 424

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₃, and A in each case corresponds to a row of Table B.

Table 425

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₃, and A in each case corresponds to a row of Table B.

Table 426

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCHCH₂, and A in each case corresponds to a row of Table B.

Table 427

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes ethoxy, and A in each case corresponds to a row of Table B.

Table 428

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a row of Table B.

Table 429

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂CH═CH₂, and A in each case corresponds to a row of Table B.

Table 430

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂CCH, and A in each case corresponds to a row of Table B.

Table 431

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂OCH₃, and A in each case corresponds to a row of Table B.

Table 432

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a row of Table B.

Table 433

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂SCH₃, and A in each case corresponds to a row of Table B.

Table 434

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a row of Table B.

Table 435

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂S(═O)CH₃, and A in each case corresponds to a row of Table B.

Table 436

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a row of Table B.

Table 437

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a row of Table B.

Table 438

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table B.

Table 439

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a row of Table B.

Table 440

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table B.

Table 441

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a row of Table B.

Table 442

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a row of Table B.

Table 443

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OC(═O)CF₃, and A in each case corresponds to a row of Table B.

Table 444

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes NHCH₂CF₃, and A in each case corresponds to a row of Table B.

Table 445

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a row of Table B.

Table 446

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a row of Table B.

Table 447

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a row of Table B.

Table 448

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a row of Table B.

Table 449

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a row of Table B.

Table 450

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂CN, and A in each case corresponds to a row of Table B.

Table 451

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂NO₂, and A in each case corresponds to a row of Table B.

Table 452

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes cyclopropyloxy, and A in each case corresponds to a row of Table B.

Table 453

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a row of Table B.

Table 454

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a row of Table B.

Table 455

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH═NOCH₃, and A in each case corresponds to a row of Table B.

Table 456

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH═NOCH₂CH₃, and A in each case corresponds to a row of Table B.

Table 457

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a row of Table B.

Table 458

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a row of Table B.

Table 459

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a row of Table B.

Table 460

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a row of Table B.

Table 461

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a row of Table B.

Table 462

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a row of Table B.

Table 463

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CF₃, and A in each case corresponds to a row of Table B.

Table 464

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes bromine, and A in each case corresponds to a row of Table B.

Table 465

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes chlorine, and A in each case corresponds to a row of Table B.

Table 466

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₃, and A in each case corresponds to a row of Table B.

Table 467

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₃, and A in each case corresponds to a row of Table B.

Table 468

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCHCH₂, and A in each case corresponds to a row of Table B.

Table 469

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes ethoxy, and A in each case corresponds to a row of Table B.

Table 470

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a row of Table B.

Table 471

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a row of Table B.

Table 472

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂CCH, and A in each case corresponds to a row of Table B.

Table 473

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂OCH₃, and A in each case corresponds to a row of Table B.

Table 474

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a row of Table B.

Table 475

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂SCH₃, and A in each case corresponds to a row of Table B.

Table 476

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a row of Table B.

Table 477

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂S(═O)CH₃, and A in each case corresponds to a row of Table B.

Table 478

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a row of Table B.

Table 479

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a row of Table B.

Table 480

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table B.

Table 481

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a row of Table B.

Table 482

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table B.

Table 483

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a row of Table B.

Table 484

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a row of Table B.

Table 485

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OC(═O)CF₃, and A in each case corresponds to a row of Table B.

Table 486

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes NHCH₂CF₃, and A in each case corresponds to a row of Table B.

Table 487

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a row of Table B.

Table 488

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a row of Table B.

Table 489

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a row of Table B.

Table 490

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a row of Table B.

Table 491

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a row of Table B.

Table 492

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂CN, and A in each case corresponds to a row of Table B.

Table 493

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂NO₂, and A in each case corresponds to a row of Table B.

Table 494

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes cyclopropyloxy, and A in each case corresponds to a row of Table B.

Table 495

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a row of Table B.

Table 496

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a row of Table B.

Table 497

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH═NOCH₃, and A in each case corresponds to a row of Table B.

Table 498

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH═NOCH₂CH₃, and A in each case corresponds to a row of Table B.

Table 499

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a row of Table B.

Table 500

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a row of Table B.

Table 501

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a row of Table B.

Table 502

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a row of Table B.

Table 503

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a row of Table B.

Table 504

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a row of Table B.

Table 505

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CF₃, and A in each case corresponds to a row of Table B.

Table 506

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes bromine, and A in each case corresponds to a row of Table B.

Table 507

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes chlorine, and A in each case corresponds to a row of Table B.

Table 508

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₃, and A in each case corresponds to a row of Table B.

Table 509

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₃, and A in each case corresponds to a row of Table B.

Table 510

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCHCH₂, and A in each case corresponds to a row of Table B.

Table 511

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes ethoxy, and A in each case corresponds to a row of Table B.

Table 512

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a row of Table B.

Table 513

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂CH═CH₂, and A in each case corresponds to a row of Table B.

Table 514

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂CCH, and A in each case corresponds to a row of Table B.

Table 515

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂OCH₃, and A in each case corresponds to a row of Table B.

Table 516

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a row of Table B.

Table 517

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂SCH₃, and A in each case corresponds to a row of Table B.

Table 518

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a row of Table B.

Table 519

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂S(═O)CH₃, and A in each case corresponds to a row of Table B.

Table 520

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a row of Table B.

Table 521

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a row of Table B.

Table 522

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table B.

Table 523

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a row of Table B.

Table 524

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table B.

Table 525

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a row of Table B.

Table 526

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a row of Table B.

Table 527

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OC(═O)CF₃, and A in each case corresponds to a row of Table B.

Table 528

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes NHCH₂CF₃, and A in each case corresponds to a row of Table B.

Table 529

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a row of Table B.

Table 530

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a row of Table B.

Table 531

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a row of Table B.

Table 532

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a row of Table B.

Table 533

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a row of Table B.

Table 534

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂CN, and A in each case corresponds to a row of Table B.

Table 535

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂NO₂, and A in each case corresponds to a row of Table B.

Table 536

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes cyclopropyloxy, and A in each case corresponds to a row of Table B.

Table 537

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a row of Table B.

Table 538

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a row of Table B.

Table 539

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH═NOCH₃, and A in each case corresponds to a row of Table B.

Table 540

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH═NOCH₂CH₃, and A in each case corresponds to a row of Table B.

Table 541

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a row of Table B.

Table 542

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a row of Table B.

Table 543

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a row of Table B.

Table 544

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a row of Table B.

Table 545

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a row of Table B.

Table 546

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a row of Table B.

Table 547

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CF₃, and A in each case corresponds to a row of Table B.

Table 548

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes bromine, and A in each case corresponds to a row of Table B.

Table 549

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes chlorine, and A in each case corresponds to a row of Table B.

Table 550

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₃, and A in each case corresponds to a row of Table B.

Table 551

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₃, and A in each case corresponds to a row of Table B.

Table 552

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCHCH₂, and A in each case corresponds to a row of Table B.

Table 553

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes ethoxy, and A in each case corresponds to a row of Table B.

Table 554

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a row of Table B.

Table 555

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂CH═CH₂, and A in each case corresponds to a row of Table B.

Table 556

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂CCH, and A in each case corresponds to a row of Table B.

Table 557

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂OCH₃, and A in each case corresponds to a row of Table B.

Table 558

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a row of Table B.

Table 559

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂SCH₃, and A in each case corresponds to a row of Table B.

Table 560

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a row of Table B.

Table 561

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂S(═O)CH₃, and A in each case corresponds to a row of Table B.

Table 562

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a row of Table B.

Table 563

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a row of Table B.

Table 564

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table B.

Table 565

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a row of Table B.

Table 566

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table B.

Table 567

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a row of Table B.

Table 568

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a row of Table B.

Table 569

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OC(═O)CF₃, and

A in each case corresponds to a row of Table B.

Table 570

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes NHCH₂CF₃, and

A in each case corresponds to a row of Table B.

Table 571

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a row of Table B.

Table 572

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a row of Table B.

Table 573

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a row of Table B.

Table 574

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a row of Table B.

Table 575

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a row of Table B.

Table 576

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂CN, and A in each case corresponds to a row of Table B.

Table 577

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂NO₂, and

A in each case corresponds to a row of Table B.

Table 578

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes cyclopropyloxy, and A in each case corresponds to a row of Table B.

Table 579

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a row of Table B.

Table 580

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a row of Table B.

Table 581

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH═NOCH₃, and A in each case corresponds to a row of Table B.

Table 582

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH═NOCH₂OH₃, and A in each case corresponds to a row of Table B.

Table 583

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a row of Table B.

Table 584

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a row of Table B.

Table 585

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a row of Table B.

Table 586

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a row of Table B.

Table 587

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a row of Table B.

Table 588

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a row of Table B.

TABLE B No. A R^(a#) R^(d) IA-136

H

IA-137 A².2 CH₃

IA-138 A².2 CH(CH₃)₂

* denotes the binding site. Table 589

Compounds of the formula IA (as defined above) wherein Q¹ denotes hydrogen, Q³ denotes CF₃, and A in each case corresponds to a row of Table C.

Table 590

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes bromine, and A in each case corresponds to a row of Table C.

Table 591

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes chlorine, and A in each case corresponds to a row of Table C.

Table 592

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₃, and A in each case corresponds to a row of Table C.

Table 593

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₃, and A in each case corresponds to a row of Table C.

Table 594

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCHCH₂, and A in each case corresponds to a row of Table C.

Table 595

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes ethoxy, and A in each case corresponds to a row of Table C.

Table 596

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a row of Table C.

Table 597

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂CH═CH₂, and A in each case corresponds to a row of Table C.

Table 598

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂CCH, and A in each case corresponds to a row of Table C.

Table 599

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂OCH₃, and A in each case corresponds to a row of Table C.

Table 600

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 601

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂SCH₃, and A in each case corresponds to a row of Table C.

Table 602

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 603

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂S(═O)CH₃, and A in each case corresponds to a row of Table C.

Table 604

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a row of Table C.

Table 605

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a row of Table C.

Table 606

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table C.

Table 607

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a row of Table C.

Table 608

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table C.

Table 609

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a row of Table C.

Table 610

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a row of Table C.

Table 611

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OC(═O)CF₃, and A in each case corresponds to a row of Table C.

Table 612

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes NHCH₂CF₃, and A in each case corresponds to a row of Table C.

Table 613

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a row of Table C.

Table 614

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a row of Table C.

Table 615

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a row of Table C.

Table 616

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a row of Table C.

Table 617

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a row of Table C.

Table 618

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂CN, and A in each case corresponds to a row of Table C.

Table 619

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂NO₂, and A in each case corresponds to a row of Table C.

Table 620

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes cyclopropyloxy, and A in each case corresponds to a row of Table C.

Table 621

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a row of Table C.

Table 622

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a row of Table C.

Table 623

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH═NOCH₃, and A in each case corresponds to a row of Table C.

Table 624

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH═NOCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 625

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a row of Table C.

Table 626

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a row of Table C.

Table 627

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a row of Table C.

Table 628

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 629

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a row of Table C.

Table 630

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a row of Table C.

Table 631

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CF₃, and A in each case corresponds to a row of Table C.

Table 632

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes bromine, and A in each case corresponds to a row of Table C.

Table 633

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes chlorine, and A in each case corresponds to a row of Table C.

Table 634

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₃, and A in each case corresponds to a row of Table C.

Table 635

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₃, and A in each case corresponds to a row of Table C.

Table 636

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCHCH₂, and A in each case corresponds to a row of Table C.

Table 637

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes ethoxy, and A in each case corresponds to a row of Table C.

Table 638

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a row of Table C.

Table 639

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂CH═CH₂, and A in each case corresponds to a row of Table C.

Table 640

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂CCH, and A in each case corresponds to a row of Table C.

Table 641

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂OCH₃, and A in each case corresponds to a row of Table C.

Table 642

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 643

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂SCH₃, and A in each case corresponds to a row of Table C.

Table 644

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 645

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂S(═O)CH₃, and A in each case corresponds to a row of Table C.

Table 646

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a row of Table C.

Table 647

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a row of Table C.

Table 648

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table C.

Table 649

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a row of Table C.

Table 650

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table C.

Table 651

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a row of Table C.

Table 652

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a row of Table C.

Table 653

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OC(═O)CF₃, and A in each case corresponds to a row of Table C.

Table 654

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes NHCH₂CF₃, and A in each case corresponds to a row of Table C.

Table 655

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a row of Table C.

Table 656

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a row of Table C.

Table 657

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a row of Table C.

Table 658

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a row of Table C.

Table 659

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a row of Table C.

Table 660

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂CN, and A in each case corresponds to a row of Table C.

Table 661

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂NO₂, and A in each case corresponds to a row of Table C.

Table 662

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes cyclopropyloxy, and A in each case corresponds to a row of Table C.

Table 663

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a row of Table C.

Table 664

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a row of Table C.

Table 665

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH═NOCH₃, and A in each case corresponds to a row of Table C.

Table 666

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH═NOCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 667

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a row of Table C.

Table 668

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a row of Table C.

Table 669

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a row of Table C.

Table 670

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 671

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a row of Table C.

Table 672

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a row of Table C.

Table 673

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CF₃, and A in each case corresponds to a row of Table C.

Table 674

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes bromine, and A in each case corresponds to a row of Table C.

Table 675

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes chlorine, and A in each case corresponds to a row of Table C.

Table 676

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₃, and A in each case corresponds to a row of Table C.

Table 677

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₃, and A in each case corresponds to a row of Table C.

Table 678

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCHCH₂, and A in each case corresponds to a row of Table C.

Table 679

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes ethoxy, and A in each case corresponds to a row of Table C.

Table 680

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a row of Table C.

Table 681

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂CH═CH₂, and A in each case corresponds to a row of Table C.

Table 682

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂CCH, and A in each case corresponds to a row of Table C.

Table 683

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂OCH₃, and A in each case corresponds to a row of Table C.

Table 684

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 685

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂SCH₃, and A in each case corresponds to a row of Table C.

Table 686

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 687

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂S(═O)CH₃, and A in each case corresponds to a row of Table C.

Table 688

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a row of Table C.

Table 689

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a row of Table C.

Table 690

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table C.

Table 691

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a row of Table C.

Table 692

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table C.

Table 693

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a row of Table C.

Table 694

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a row of Table C.

Table 695

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OC(═O)CF₃, and A in each case corresponds to a row of Table C.

Table 696

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes NHCH₂CF₃, and A in each case corresponds to a row of Table C.

Table 697

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a row of Table C.

Table 698

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a row of Table C.

Table 699

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a row of Table C.

Table 700

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a row of Table C.

Table 701

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a row of Table C.

Table 702

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂CN, and A in each case corresponds to a row of Table C.

Table 703

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂NO₂, and A in each case corresponds to a row of Table C.

Table 704

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes cyclopropyloxy, and A in each case corresponds to a row of Table C.

Table 705

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a row of Table C.

Table 706

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a row of Table C.

Table 707

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH═NOCH₃, and A in each case corresponds to a row of Table C.

Table 708

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH═NOCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 709

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a row of Table C.

Table 710

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a row of Table C.

Table 711

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a row of Table C.

Table 712

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 713

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a row of Table C.

Table 714

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a row of Table C.

Table 715

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CF₃, and A in each case corresponds to a row of Table C.

Table 716

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes bromine, and A in each case corresponds to a row of Table C.

Table 717

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes chlorine, and A in each case corresponds to a row of Table C.

Table 718

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₃, and A in each case corresponds to a row of Table C.

Table 719

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₃, and A in each case corresponds to a row of Table C.

Table 720

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCHCH₂, and A in each case corresponds to a row of Table C.

Table 721

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes ethoxy, and A in each case corresponds to a row of Table C.

Table 722

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a row of Table C.

Table 723

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂CH═CH₂, and A in each case corresponds to a row of Table C.

Table 724

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂CCH, and A in each case corresponds to a row of Table C.

Table 725

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂OCH₃, and A in each case corresponds to a row of Table C.

Table 726

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 727

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂SCH₃, and A in each case corresponds to a row of Table C.

Table 728

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 729

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂S(═O)CH₁₃, and A in each case corresponds to a row of Table C.

Table 730

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a row of Table C.

Table 731

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a row of Table C.

Table 732

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table C.

Table 733

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a row of Table C.

Table 734

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table C.

Table 735

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a row of Table C.

Table 736

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a row of Table C.

Table 737

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OC(═O)CF₃, and A in each case corresponds to a row of Table C.

Table 738

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes NHCH₂CF₃, and A in each case corresponds to a row of Table C.

Table 739

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a row of Table C.

Table 740

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a row of Table C.

Table 741

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a row of Table C.

Table 742

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a row of Table C.

Table 743

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a row of Table C.

Table 744

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂CN, and A in each case corresponds to a row of Table C.

Table 745

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂NO₂, and A in each case corresponds to a row of Table C.

Table 746

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes cyclopropyloxy, and A in each case corresponds to a row of Table C.

Table 747

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a row of Table C.

Table 748

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a row of Table C.

Table 749

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH═NOCH₃, and A in each case corresponds to a row of Table C.

Table 750

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH═NOCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 751

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a row of Table C.

Table 752

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a row of Table C.

Table 753

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a row of Table C.

Table 754

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 755

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a row of Table C.

Table 756

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a row of Table C.

Table 757

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CF₃, and A in each case corresponds to a row of Table C.

Table 758

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes bromine, and A in each case corresponds to a row of Table C.

Table 759

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes chlorine, and A in each case corresponds to a row of Table C.

Table 760

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₃, and A in each case corresponds to a row of Table C.

Table 761

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₃, and A in each case corresponds to a row of Table C.

Table 762

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCHCH₂, and A in each case corresponds to a row of Table C.

Table 763

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes ethoxy, and A in each case corresponds to a row of Table C.

Table 764

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a row of Table C.

Table 765

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂CH═CH₂, and A in each case corresponds to a row of Table C.

Table 766

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂CCH, and A in each case corresponds to a row of Table C.

Table 767

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂OCH₃, and A in each case corresponds to a row of Table C.

Table 768

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 769

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂SCH₃, and A in each case corresponds to a row of Table C.

Table 770

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 771

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂S(═O)CH₃, and A in each case corresponds to a row of Table C.

Table 772

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a row of Table C.

Table 773

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a row of Table C.

Table 774

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table C.

Table 775

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a row of Table C.

Table 776

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table C.

Table 777

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a row of Table C.

Table 778

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a row of Table C.

Table 779

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OC(═O)CF₃, and A in each case corresponds to a row of Table C.

Table 780

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes NHCH₂CF₃, and A in each case corresponds to a row of Table C.

Table 781

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a row of Table C.

Table 782

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a row of Table C.

Table 783

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a row of Table C.

Table 784

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a row of Table C.

Table 785

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a row of Table C.

Table 786

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂CN, and A in each case corresponds to a row of Table C.

Table 787

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂NO₂, and A in each case corresponds to a row of Table C.

Table 788

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes cyclopropyloxy, and A in each case corresponds to a row of Table C.

Table 789

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a row of Table C.

Table 790

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a row of Table C.

Table 791

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH═NOCH₃, and A in each case corresponds to a row of Table C.

Table 792

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH═NOCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 793

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a row of Table C.

Table 794

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a row of Table C.

Table 795

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a row of Table C.

Table 796

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 797

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a row of Table C.

Table 798

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a row of Table C.

Table 799

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CF₃, and A in each case corresponds to a row of Table C.

Table 800

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes bromine, and A in each case corresponds to a row of Table C.

Table 801

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes chlorine, and A in each case corresponds to a row of Table C.

Table 802

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₃, and A in each case corresponds to a row of Table C.

Table 803

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₃, and A in each case corresponds to a row of Table C.

Table 804

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCHCH₂, and A in each case corresponds to a row of Table C.

Table 805

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes ethoxy, and A in each case corresponds to a row of Table C.

Table 806

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a row of Table C.

Table 807

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂CH═CH₂, and A in each case corresponds to a row of Table C.

Table 808

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂CCH, and A in each case corresponds to a row of Table C.

Table 809

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂OCH₃, and A in each case corresponds to a row of Table C.

Table 810

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 811

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂SCH₃, and A in each case corresponds to a row of Table C.

Table 812

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 813

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂S(═O)CH₃, and A in each case corresponds to a row of Table C.

Table 814

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a row of Table C.

Table 815

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a row of Table C.

Table 816

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table C.

Table 817

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a row of Table C.

Table 818

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table C.

Table 819

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a row of Table C.

Table 820

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a row of Table C.

Table 821

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OC(═O)CF₃, and A in each case corresponds to a row of Table C.

Table 822

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes NHCH₂CF₃, and A in each case corresponds to a row of Table C.

Table 823

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a row of Table C.

Table 824

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a row of Table C.

Table 825

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a row of Table C.

Table 826

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a row of Table C.

Table 827

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a row of Table C.

Table 828

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂CN, and A in each case corresponds to a row of Table C.

Table 829

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂NO₂, and A in each case corresponds to a row of Table C.

Table 830

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes cyclopropyloxy, and A in each case corresponds to a row of Table C.

Table 831

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a row of Table C.

Table 832

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a row of Table C.

Table 833

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH═NOCH₃, and A in each case corresponds to a row of Table C.

Table 834

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH═NOCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 835

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a row of Table C.

Table 836

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a row of Table C.

Table 837

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a row of Table C.

Table 838

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 839

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a row of Table C.

Table 840

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a row of Table C.

Table 841

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CF₃, and A in each case corresponds to a row of Table C.

Table 842

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes bromine, and A in each case corresponds to a row of Table C.

Table 843

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes chlorine, and A in each case corresponds to a row of Table C.

Table 844

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₃, and A in each case corresponds to a row of Table C.

Table 845

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₃, and A in each case corresponds to a row of Table C.

Table 846

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCHCH₂, and A in each case corresponds to a row of Table C.

Table 847

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes ethoxy, and A in each case corresponds to a row of Table C.

Table 848

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a row of Table C.

Table 849

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂CH═CH₂, and A in each case corresponds to a row of Table C.

Table 850

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂CCH, and A in each case corresponds to a row of Table C.

Table 851

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂OCH₃, and A in each case corresponds to a row of Table C.

Table 852

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 853

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂SCH₃, and A in each case corresponds to a row of Table C.

Table 854

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 855

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂S(═O)CH₃, and A in each case corresponds to a row of Table C.

Table 856

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a row of Table C.

Table 857

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a row of Table C.

Table 858

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table C.

Table 859

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a row of Table C.

Table 860

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a row of Table C.

Table 861

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a row of Table C.

Table 862

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a row of Table C.

Table 863

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OC(═O)CF₃, and A in each case corresponds to a row of Table C.

Table 864

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes NHCH₂CF₃, and A in each case corresponds to a row of Table C.

Table 865

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a row of Table C.

Table 866

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a row of Table C.

Table 867

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a row of Table C.

Table 868

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a row of Table C.

Table 869

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a row of Table C.

Table 870

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂CN, and A in each case corresponds to a row of Table C.

Table 871

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂NO₂, and A in each case corresponds to a row of Table C.

Table 872

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes cyclopropyloxy, and A in each case corresponds to a row of Table C.

Table 873

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a row of Table C.

Table 874

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a row of Table C.

Table 875

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH═NOCH₃, and A in each case corresponds to a row of Table C.

Table 876

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH═NOCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 877

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a row of Table C.

Table 878

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a row of Table C.

Table 879

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a row of Table C.

Table 880

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a row of Table C.

Table 881

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a row of Table C.

Table 882

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a row of Table C.

TABLE C No. A R^(e) R^(f) IA-139

CH₃ CH₃ IA-140 A¹.1 CH₂CH₃ CH₃ IA-141 A¹.1 CH═CH₂ CH₃ IA-142 A¹.1 CH₂CH₂CH₃ CH₃ IA-143 A¹.1 CH(CH₃)₂ CH₃ IA-144 A¹.1 CH₂CH₂CH₂CH₃ CH₃ IA-145 A¹.1 C(CH₃)₃ CH₃ IA-146 A¹.1 CH₂CH(CH₃)₂ CH₃ IA-147 A¹.1 CH(CH₃)CH₂CH₃ CH₃ IA-148 A¹.1 CH₂CHCH₂ CH₃ IA-149 A¹.1 CH₂CCH CH₃ IA-150 A¹.1 CH(CH₃)CH═CH₂ CH₃ IA-151 A¹.1 CHF₂ CH₃ IA-152 A¹.1 CH₂Cl CH₃ IA-153 A¹.1 CH₂CH₂CN CH₃ IA-154 A¹.1 CH₂CH₂Cl CH₃ IA-155 A¹.1 CH₂CH₂OH CH₃ IA-156 A¹.1 CH₂CH₂CH₂OH CH₃ IA-157 A¹.1 CH₂CH(OH)CH₂OH CH₃ IA-158 A¹.1 CH₂CH(OCH₃)₂ CH₃ IA-159 A¹.1 CH₂SCH₃ CH₃ IA-160 A¹.1 (CH₂)₃SCH₃ CH₃ IA-161 A¹.1 CH₂S(═O)CH₃ CH₃ IA-162 A¹.1 CH₂S(═O)₂CH₃ CH₃ IA-163 A¹.1 CH₂C(═O)CH₃ CH₃ IA-164 A¹.1 CH₂C(═O)CH₂CH₃ CH₃ IA-165 A¹.1 CH₂COOH CH₃ IA-166 A¹.1 CH₂COOCH₃ CH₃ IA-167 A¹.1 CH₂COOCH₂CH₃ CH₃ IA-168 A¹.1 cyclo-C₃H₅ CH₃ IA-169 A¹.1 cyclo-C₄H₇ CH₃ IA-170 A¹.1 cyclo-C₅H₉ CH₃ IA-171 A¹.1 cyclo-C₆H₁₁ CH₃ IA-172 A¹.1 C₆H₅ CH₃ IA-173 A¹.1 CH₂CH₃ CH₂CH₃ IA-174 A¹.1 CH═CH₂ CH₂CH₃ IA-175 A¹.1 CH₂CH₂CH₃ CH₂CH₃ IA-176 A¹.1 CH(CH₃)₂ CH₂CH₃ IA-177 A¹.1 CH₂CH₂CH₂CH₃ CH₂CH₃ IA-178 A¹.1 C(CH₃)₃ CH₂CH₃ IA-179 A¹.1 CH₂CH(CH₃)₂ CH₂CH₃ IA-180 A¹.1 CH(CH₃)CH₂CH₃ CH₂CH₃ IA-181 A¹.1 CH₂CHCH₂ CH₂CH₃ IA-182 A¹.1 CH₂CCH CH₂CH₃ IA-183 A¹.1 CH(CH₃)CH═CH₂ CH₂CH₃ IA-184 A¹.1 CHF₂ CH₂CH₃ IA-185 A¹.1 CH₂Cl CH₂CH₃ IA-186 A¹.1 CH₂CH₂CN CH₂CH₃ IA-187 A¹.1 CH₂CH₂Cl CH₂CH₃ IA-188 A¹.1 CH₂CH₂OH CH₂CH₃ IA-189 A¹.1 CH₂CH₂CH₂OH CH₂CH₃ IA-190 A¹.1 CH₂CH(OH)CH₂OH CH₂CH₃ IA-191 A¹.1 CH₂CH(OCH₃)₂ CH₂CH₃ IA-192 A¹.1 CH₂SCH₃ CH₂CH₃ IA-193 A¹.1 (CH₂)₃SCH₃ CH₂CH₃ IA-194 A¹.1 CH₂S(═O)CH₃ CH₂CH₃ IA-195 A¹.1 CH₂S(═O)₂CH₃ CH₂CH₃ IA-196 A¹.1 CH₂C(═O)CH₃ CH₂CH₃ IA-197 A¹.1 CH₂C(═O)CH₂CH₃ CH₂CH₃ IA-198 A¹.1 CH₂COOH CH₂CH₃ IA-199 A¹.1 CH₂COOCH₃ CH₂CH₃ IA-200 A¹.1 CH₂COOCH₂CH₃ CH₂CH₃ IA-201 A¹.1 cyclo-C₃H₅ CH₂CH₃ IA-202 A¹.1 cyclo-C₄H₇ CH₂CH₃ IA-203 A¹.1 cyclo-C₅H₉ CH₂CH₃ IA-204 A¹.1 cyclo-C₆H₁₁ CH₂CH₃ IA-205 A¹.1 C₆H₅ CH₂CH₃ IA-206 A¹.1 CH═CH₂ CH═CH₂ IA-207 A¹.1 CH₂CH₂CH₃ CH═CH₂ IA-208 A¹.1 CH(CH₃)₂ CH═CH₂ IA-209 A¹.1 CH₂CH₂CH₂CH₃ CH═CH₂ IA-210 A¹.1 C(CH₃)₃ CH═CH₂ IA-211 A¹.1 CH₂CH(CH₃)₂ CH═CH₂ IA-212 A¹.1 CH(CH₃)CH₂CH₃ CH═CH₂ IA-213 A¹.1 CH₂CHCH₂ CH═CH₂ IA-214 A¹.1 CH₂CCH CH═CH₂ IA-215 A¹.1 CH(CH₃)CH═CH₂ CH═CH₂ IA-216 A¹.1 CHF₂ CH═CH₂ IA-217 A¹.1 CH₂Cl CH═CH₂ IA-218 A¹.1 CH₂CH₂CN CH═CH₂ IA-219 A¹.1 CH₂CH₂Cl CH═CH₂ IA-220 A¹.1 CH₂CH₂OH CH═CH₂ IA-221 A¹.1 CH₂CH₂CH₂OH CH═CH₂ IA-222 A¹.1 CH₂CH(OH)CH₂OH CH═CH₂ IA-223 A¹.1 CH₂CH(OCH₃)₂ CH═CH₂ IA-224 A¹.1 CH₂SCH₃ CH═CH₂ IA-225 A¹.1 (CH₂)₃SCH₃ CH═CH₂ IA-226 A¹.1 CH₂S(═O)CH₃ CH═CH₂ IA-227 A¹.1 CH₂S(═O)₂CH₃ CH═CH₂ IA-228 A¹.1 CH₂C(═O)CH₃ CH═CH₂ IA-229 A¹.1 CH₂C(═O)CH₂CH₃ CH═CH₂ IA-230 A¹.1 CH₂COOH CH═CH₂ IA-231 A¹.1 CH₂COOCH₃ CH═CH₂ IA-232 A¹.1 CH₂COOCH₂CH₃ CH═CH₂ IA-233 A¹.1 cyclo-C₃H₅ CH═CH₂ IA-234 A¹.1 cyclo-C₄H₇ CH═CH₂ IA-235 A¹.1 cyclo-C₅H₉ CH═CH₂ IA-236 A¹.1 cyclo-C₆H₁₁ CH═CH₂ IA-237 A¹.1 C₆H₅ CH═CH₂ IA-238 A¹.1 CH₂CH₂CH₃ CH₂CH₂CH₃ IA-239 A¹.1 CH(CH₃)₂ CH₂CH₂CH₃ IA-240 A¹.1 CH₂CH₂CH₂CH₃ CH₂CH₂CH₃ IA-241 A¹.1 C(CH₃)₃ CH₂CH₂CH₃ IA-242 A¹.1 CH₂CH(CH₃)₂ CH₂CH₂CH₃ IA-243 A¹.1 CH(CH₃)CH₂CH₃ CH₂CH₂CH₃ IA-244 A¹.1 CH₂CHCH₂ CH₂CH₂CH₃ IA-245 A¹.1 CH₂CCH CH₂CH₂CH₃ IA-246 A¹.1 CH(CH₃)CH═CH₂ CH₂CH₂CH₃ IA-247 A¹.1 CHF₂ CH₂CH₂CH₃ IA-248 A¹.1 CH₂Cl CH₂CH₂CH₃ IA-249 A¹.1 CH₂CH₂CN CH₂CH₂CH₃ IA-250 A¹.1 CH₂CH₂Cl CH₂CH₂CH₃ IA-251 A¹.1 CH₂CH₂OH CH₂CH₂CH₃ IA-252 A¹.1 CH₂CH₂CH₂OH CH₂CH₂CH₃ IA-253 A¹.1 CH₂CH(OH)CH₂OH CH₂CH₂CH₃ IA-254 A¹.1 CH₂CH(OCH₃)₂ CH₂CH₂CH₃ IA-255 A¹.1 CH₂SCH₃ CH₂CH₂CH₃ IA-256 A¹.1 (CH₂)₃SCH₃ CH₂CH₂CH₃ IA-257 A¹.1 CH₂S(═O)CH₃ CH₂CH₂CH₃ IA-258 A¹.1 CH₂S(═O)₂CH₃ CH₂CH₂CH₃ IA-259 A¹.1 CH₂C(═O)CH₃ CH₂CH₂CH₃ IA-260 A¹.1 CH₂C(═O)CH₂CH₃ CH₂CH₂CH₃ IA-261 A¹.1 CH₂COOH CH₂CH₂CH₃ IA-262 A¹.1 CH₂COOCH₃ CH₂CH₂CH₃ IA-263 A¹.1 CH₂COOCH₂CH₃ CH₂CH₂CH₃ IA-264 A¹.1 cyclo-C₃H₅ CH₂CH₂CH₃ IA-265 A¹.1 cyclo-C₄H₇ CH₂CH₂CH₃ IA-266 A¹.1 cyclo-C₅H₉ CH₂CH₂CH₃ IA-267 A¹.1 cyclo-C₆H₁₁ CH₂CH₂CH₃ IA-268 A¹.1 C₆H₅ CH₂CH₂CH₃ IA-269 A¹.1 CH(CH₃)₂ CH(CH₃)₂ IA-270 A¹.1 CH₂CH₂CH₂CH₃ CH(CH₃)₂ IA-271 A¹.1 C(CH₃)₃ CH(CH₃)₂ IA-272 A¹.1 CH₂CH(CH₃)₂ CH(CH₃)₂ IA-273 A¹.1 CH(CH₃)CH₂CH₃ CH(CH₃)₂ IA-274 A¹.1 CH₂CHCH₂ CH(CH₃)₂ IA-275 A¹.1 CH₂CCH CH(CH₃)₂ IA-276 A¹.1 CH(CH₃)CH═CH₂ CH(CH₃)₂ IA-277 A¹.1 CHF₂ CH(CH₃)₂ IA-278 A¹.1 CH₂Cl CH(CH₃)₂ IA-279 A¹.1 CH₂CH₂CN CH(CH₃)₂ IA-280 A¹.1 CH₂CH₂Cl CH(CH₃)₂ IA-281 A¹.1 CH₂CH₂OH CH(CH₃)₂ IA-282 A¹.1 CH₂CH₂CH₂OH CH(CH₃)₂ IA-283 A¹.1 CH₂CH(OH)CH₂OH CH(CH₃)₂ IA-284 A¹.1 CH₂CH(OCH₃)₂ CH(CH₃)₂ IA-285 A¹.1 CH₂SCH₃ CH(CH₃)₂ IA-286 A¹.1 (CH₂)₃SCH₃ CH(CH₃)₂ IA-287 A¹.1 CH₂S(═O)CH₃ CH(CH₃)₂ IA-288 A¹.1 CH₂S(═O)₂CH₃ CH(CH₃)₂ IA-289 A¹.1 CH₂C(═O)CH₃ CH(CH₃)₂ IA-290 A¹.1 CH₂C(═O)CH₂CH₃ CH(CH₃)₂ IA-291 A¹.1 CH₂COOH CH(CH₃)₂ IA-292 A¹.1 CH₂COOCH₃ CH(CH₃)₂ IA-293 A¹.1 CH₂COOCH₂CH₃ CH(CH₃)₂ IA-294 A¹.1 cyclo-C₃H₅ CH(CH₃)₂ IA-295 A¹.1 cyclo-C₄H₇ CH(CH₃)₂ IA-296 A¹.1 cyclo-C₅H₉ CH(CH₃)₂ IA-297 A¹.1 cyclo-C₆H₁₁ CH(CH₃)₂ IA-298 A¹.1 C₆H₅ CH(CH₃)₂ IA-299 A¹.1 CH₂CH₂CH₂CH₃ CH₂CH₂CH₂CH₃ IA-300 A¹.1 C(CH₃)₃ CH₂CH₂CH₂CH₃ IA-301 A¹.1 CH₂CH(CH₃)₂ CH₂CH₂CH₂CH₃ IA-302 A¹.1 CH(CH₃)CH₂CH₃ CH₂CH₂CH₂CH₃ IA-303 A¹.1 CH₂CHCH₂ CH₂CH₂CH₂CH₃ IA-304 A¹.1 CH₂CCH CH₂CH₂CH₂CH₃ IA-305 A¹.1 CH(CH₃)CH═CH₂ CH₂CH₂CH₂CH₃ IA-306 A¹.1 CHF₂ CH₂CH₂CH₂CH₃ IA-307 A¹.1 CH₂Cl CH₂CH₂CH₂CH₃ IA-308 A¹.1 CH₂CH₂CN CH₂CH₂CH₂CH₃ IA-309 A¹.1 CH₂CH₂Cl CH₂CH₂CH₂CH₃ IA-310 A¹.1 CH₂CH₂OH CH₂CH₂CH₂CH₃ IA-311 A¹.1 CH₂CH₂CH₂OH CH₂CH₂CH₂CH₃ IA-312 A¹.1 CH₂CH(OH)CH₂OH CH₂CH₂CH₂CH₃ IA-313 A¹.1 CH₂CH(OCH₃)₂ CH₂CH₂CH₂CH₃ IA-314 A¹.1 CH₂SCH₃ CH₂CH₂CH₂CH₃ IA-315 A¹.1 (CH₂)₃SCH₃ CH₂CH₂CH₂CH₃ IA-316 A¹.1 CH₂S(═O)CH₃ CH₂CH₂CH₂CH₃ IA-317 A¹.1 CH₂S(═O)₂CH₃ CH₂CH₂CH₂CH₃ IA-318 A¹.1 CH₂C(═O)CH₃ CH₂CH₂CH₂CH₃ IA-319 A¹.1 CH₂C(═O)CH₂CH₃ CH₂CH₂CH₂CH₃ IA-320 A¹.1 CH₂COOH CH₂CH₂CH₂CH₃ IA-321 A¹.1 CH₂COOCH₃ CH₂CH₂CH₂CH₃ IA-322 A¹.1 CH₂COOCH₂CH₃ CH₂CH₂CH₂CH₃ IA-323 A¹.1 cyclo-C₃H₅ CH₂CH₂CH₂CH₃ IA-324 A¹.1 cyclo-C₄H₇ CH₂CH₂CH₂CH₃ IA-325 A¹.1 cyclo-C₅H₉ CH₂CH₂CH₂CH₃ IA-326 A¹.1 cyclo-C₆H₁₁ CH₂CH₂CH₂CH₃ IA-327 A¹.1 C₆H₅ CH₂CH₂CH₂CH₃ IA-328 A¹.1 C(CH₃)₃ C(CH₃)₃ IA-329 A¹.1 CH₂CH(CH₃)₂ C(CH₃)₃ IA-330 A¹.1 CH(CH₃)CH₂CH₃ C(CH₃)₃ IA-331 A¹.1 CH₂CHCH₂ C(CH₃)₃ IA-332 A¹.1 CH₂CCH C(CH₃)₃ IA-333 A¹.1 CH(CH₃)CH═CH₂ C(CH₃)₃ IA-334 A¹.1 CHF₂ C(CH₃)₃ IA-335 A¹.1 CH₂Cl C(CH₃)₃ IA-336 A¹.1 CH₂CH₂CN C(CH₃)₃ IA-337 A¹.1 CH₂CH₂Cl C(CH₃)₃ IA-338 A¹.1 CH₂CH₂OH C(CH₃)₃ IA-339 A¹.1 CH₂CH₂CH₂OH C(CH₃)₃ IA-340 A¹.1 CH₂CH(OH)CH₂OH C(CH₃)₃ IA-341 A¹.1 CH₂CH(OCH₃)₂ C(CH₃)₃ IA-342 A¹.1 CH₂SCH₃ C(CH₃)₃ IA-343 A¹.1 (CH₂)₃SCH₃ C(CH₃)₃ IA-344 A¹.1 CH₂S(═O)CH₃ C(CH₃)₃ IA-345 A¹.1 CH₂S(═O)₂CH₃ C(CH₃)₃ IA-346 A¹.1 CH₂C(═O)CH₃ C(CH₃)₃ IA-347 A¹.1 CH₂C(═O)CH₂CH₃ C(CH₃)₃ IA-348 A¹.1 CH₂COOH C(CH₃)₃ IA-349 A¹.1 CH₂COOCH₃ C(CH₃)₃ IA-350 A¹.1 CH₂COOCH₂CH₃ C(CH₃)₃ IA-351 A¹.1 cyclo-C₃H₅ C(CH₃)₃ IA-352 A¹.1 cyclo-C₄H₇ C(CH₃)₃ IA-353 A¹.1 cyclo-C₅H₉ C(CH₃)₃ IA-354 A¹.1 cyclo-C₆H₁₁ C(CH₃)₃ IA-355 A¹.1 C₆H₅ C(CH₃)₃ IA-356 A¹.1 CH₂CH(CH₃)₂ CH₂CH(CH₃)₂ IA-357 A¹.1 CH(CH₃)CH₂CH₃ CH₂CH(CH₃)₂ IA-358 A¹.1 CH₂CHCH₂ CH₂CH(CH₃)₂ IA-359 A¹.1 CH₂CCH CH₂CH(CH₃)₂ IA-360 A¹.1 CH(CH₃)CH═CH₂ CH₂CH(CH₃)₂ IA-361 A¹.1 CHF₂ CH₂CH(CH₃)₂ IA-362 A¹.1 CH₂Cl CH₂CH(CH₃)₂ IA-363 A¹.1 CH₂CH₂CN CH₂CH(CH₃)₂ IA-364 A¹.1 CH₂CH₂Cl CH₂CH(CH₃)₂ IA-365 A¹.1 CH₂CH₂OH CH₂CH(CH₃)₂ IA-366 A¹.1 CH₂CH₂CH₂OH CH₂CH(CH₃)₂ IA-367 A¹.1 CH₂CH(OH)CH₂OH CH₂CH(CH₃)₂ IA-368 A¹.1 CH₂CH(OCH₃)₂ CH₂CH(CH₃)₂ IA-369 A¹.1 CH₂SCH₃ CH₂CH(CH₃)₂ IA-370 A¹.1 (CH₂)₃SCH₃ CH₂CH(CH₃)₂ IA-371 A¹.1 CH₂S(═O)CH₃ CH₂CH(CH₃)₂ IA-372 A¹.1 CH₂S(═O)₂CH₃ CH₂CH(CH₃)₂ IA-373 A¹.1 CH₂C(═O)CH₃ CH₂CH(CH₃)₂ IA-374 A¹.1 CH₂C(═O)CH₂CH₃ CH₂CH(CH₃)₂ IA-375 A¹.1 CH₂COOH CH₂CH(CH₃)₂ IA-376 A¹.1 CH₂COOCH₃ CH₂CH(CH₃)₂ IA-377 A¹.1 CH₂COOCH₂CH₃ CH₂CH(CH₃)₂ IA-378 A¹.1 cyclo-C₃H₅ CH₂CH(CH₃)₂ IA-379 A¹.1 cyclo-C₄H₇ CH₂CH(CH₃)₂ IA-380 A¹.1 cyclo-C₅H₉ CH₂CH(CH₃)₂ IA-381 A¹.1 cyclo-C₆H₁₁ CH₂CH(CH₃)₂ IA-382 A¹.1 C₆H₅ CH₂CH(CH₃)₂ IA-383 A¹.1 CH(CH₃)CH₂CH₃ CH(CH₃)CH₂CH₃ IA-384 A¹.1 CH₂CHCH₂ CH(CH₃)CH₂CH₃ IA-385 A¹.1 CH₂CCH CH(CH₃)CH₂CH₃ IA-386 A¹.1 CH(CH₃)CH═CH₂ CH(CH₃)CH₂CH₃ IA-387 A¹.1 CHF₂ CH(CH₃)CH₂CH₃ IA-388 A¹.1 CH₂Cl CH(CH₃)CH₂CH₃ IA-389 A¹.1 CH₂CH₂CN CH(CH₃)CH₂CH₃ IA-390 A¹.1 CH₂CH₂Cl CH(CH₃)CH₂CH₃ IA-391 A¹.1 CH₂CH₂OH CH(CH₃)CH₂CH₃ IA-392 A¹.1 CH₂CH₂CH₂OH CH(CH₃)CH₂CH₃ IA-393 A¹.1 CH₂CH(OH)CH₂OH CH(CH₃)CH₂CH₃ IA-394 A¹.1 CH₂CH(OCH₃)₂ CH(CH₃)CH₂CH₃ IA-395 A¹.1 CH₂SCH₃ CH(CH₃)CH₂CH₃ IA-396 A¹.1 (CH₂)₃SCH₃ CH(CH₃)CH₂CH₃ IA-397 A¹.1 CH₂S(═O)CH₃ CH(CH₃)CH₂CH₃ IA-398 A¹.1 CH₂S(═O)₂CH₃ CH(CH₃)CH₂CH₃ IA-399 A¹.1 CH₂C(═O)CH₃ CH(CH₃)CH₂CH₃ IA-400 A¹.1 CH₂C(═O)CH₂CH₃ CH(CH₃)CH₂CH₃ IA-401 A¹.1 CH₂COOH CH(CH₃)CH₂CH₃ IA-402 A¹.1 CH₂COOCH₃ CH(CH₃)CH₂CH₃ IA-403 A¹.1 CH₂COOCH₂CH₃ CH(CH₃)CH₂CH₃ IA-404 A¹.1 cyclo-C₃H₅ CH(CH₃)CH₂CH₃ IA-405 A¹.1 cyclo-C₄H₇ CH(CH₃)CH₂CH₃ IA-406 A¹.1 cyclo-C₅H₉ CH(CH₃)CH₂CH₃ IA-407 A¹.1 cyclo-C₆H₁₁ CH(CH₃)CH₂CH₃ IA-408 A¹.1 C₆H₅ CH(CH₃)CH₂CH₃ IA-409 A¹.1 CH₂CHCH₂ CH₂CHCH₂ IA-410 A¹.1 CH₂CCH CH₂CHCH₂ IA-411 A¹.1 CH(CH₃)CH═CH₂ CH₂CHCH₂ IA-412 A¹.1 CHF₂ CH₂CHCH₂ IA-413 A¹.1 CH₂Cl CH₂CHCH₂ IA-414 A¹.1 CH₂CH₂CN CH₂CHCH₂ IA-415 A¹.1 CH₂CH₂Cl CH₂CHCH₂ IA-416 A¹.1 CH₂CH₂OH CH₂CHCH₂ IA-417 A¹.1 CH₂CH₂CH₂OH CH₂CHCH₂ IA-418 A¹.1 CH₂CH(OH)CH₂OH CH₂CHCH₂ IA-419 A¹.1 CH₂CH(OCH₃)₂ CH₂CHCH₂ IA-420 A¹.1 CH₂SCH₃ CH₂CHCH₂ IA-421 A¹.1 (CH₂)₃SCH₃ CH₂CHCH₂ IA-422 A¹.1 CH₂S(═O)CH₃ CH₂CHCH₂ IA-423 A¹.1 CH₂S(═O)₂CH₃ CH₂CHCH₂ IA-424 A¹.1 CH₂C(═O)CH₃ CH₂CHCH₂ IA-425 A¹.1 CH₂C(═O)CH₂CH₃ CH₂CHCH₂ IA-426 A¹.1 CH₂COOH CH₂CHCH₂ IA-427 A¹.1 CH₂COOCH₃ CH₂CHCH₂ IA-428 A¹.1 CH₂COOCH₂CH₃ CH₂CHCH₂ IA-429 A¹.1 cyclo-C₃H₅ CH₂CHCH₂ IA-430 A¹.1 cyclo-C₄H₇ CH₂CHCH₂ IA-431 A¹.1 cyclo-C₅H₉ CH₂CHCH₂ IA-432 A¹.1 cyclo-C₆H₁₁ CH₂CHCH₂ IA-433 A¹.1 C₆H₅ CH₂CHCH₂ IA-434 A¹.1 CH₂CCH CH₂CCH IA-435 A¹.1 CH(CH₃)CH═CH₂ CH₂CCH IA-436 A¹.1 CHF₂ CH₂CCH IA-437 A¹.1 CH₂Cl CH₂CCH IA-438 A¹.1 CH₂CH₂CN CH₂CCH IA-439 A¹.1 CH₂CH₂Cl CH₂CCH IA-440 A¹.1 CH₂CH₂OH CH₂CCH IA-441 A¹.1 CH₂CH₂CH₂OH CH₂CCH IA-442 A¹.1 CH₂CH(OH)CH₂OH CH₂CCH IA-443 A¹.1 CH₂CH(OCH₃)₂ CH₂CCH IA-444 A¹.1 CH₂SCH₃ CH₂CCH IA-445 A¹.1 (CH₂)₃SCH₃ CH₂CCH IA-446 A¹.1 CH₂S(═O)CH₃ CH₂CCH IA-447 A¹.1 CH₂S(═O)₂CH₃ CH₂CCH IA-448 A¹.1 CH₂C(═O)CH₃ CH₂CCH IA-449 A¹.1 CH₂C(═O)CH₂CH₃ CH₂CCH IA-450 A¹.1 CH₂COOH CH₂CCH IA-451 A¹.1 CH₂COOCH₃ CH₂CCH IA-452 A¹.1 CH₂COOCH₂CH₃ CH₂CCH IA-453 A¹.1 cyclo-C₃H₅ CH₂CCH IA-454 A¹.1 cyclo-C₄H₇ CH₂CCH IA-455 A¹.1 cyclo-C₅H₉ CH₂CCH IA-456 A¹.1 cyclo-C₆H₁₁ CH₂CCH IA-457 A¹.1 C₆H₅ CH₂CCH IA-458 A¹.1 CH(CH₃)CH═CH₂ CH(CH₃)CH═CH₂ IA-459 A¹.1 CHF₂ CH(CH₃)CH═CH₂ IA-460 A¹.1 CH₂Cl CH(CH₃)CH═CH₂ IA-461 A¹.1 CH₂CH₂CN CH(CH₃)CH═CH₂ IA-462 A¹.1 CH₂CH₂Cl CH(CH₃)CH═CH₂ IA-463 A¹.1 CH₂CH₂OH CH(CH₃)CH═CH₂ IA-464 A¹.1 CH₂CH₂CH₂OH CH(CH₃)CH═CH₂ IA-465 A¹.1 CH₂CH(OH)CH₂OH CH(CH₃)CH═CH₂ IA-466 A¹.1 CH₂CH(OCH₃)₂ CH(CH₃)CH═CH₂ IA-467 A¹.1 CH₂SCH₃ CH(CH₃)CH═CH₂ IA-468 A¹.1 (CH₂)₃SCH₃ CH(CH₃)CH═CH₂ IA-469 A¹.1 CH₂S(═O)CH₃ CH(CH₃)CH═CH₂ IA-470 A¹.1 CH₂S(═O)₂CH₃ CH(CH₃)CH═CH₂ IA-471 A¹.1 CH₂C(═O)CH₃ CH(CH₃)CH═CH₂ IA-472 A¹.1 CH₂C(═O)CH₂CH₃ CH(CH₃)CH═CH₂ IA-473 A¹.1 CH₂COOH CH(CH₃)CH═CH₂ IA-474 A¹.1 CH₂COOCH₃ CH(CH₃)CH═CH₂ IA-475 A¹.1 CH₂COOCH₂CH₃ CH(CH₃)CH═CH₂ IA-476 A¹.1 cyclo-C₃H₅ CH(CH₃)CH═CH₂ IA-477 A¹.1 cyclo-C₄H₇ CH(CH₃)CH═CH₂ IA-478 A¹.1 cyclo-C₅H₉ CH(CH₃)CH═CH₂ IA-479 A¹.1 cyclo-C₆H₁₁ CH(CH₃)CH═CH₂ IA-480 A¹.1 C₆H₅ CH(CH₃)CH═CH₂ IA-481 A¹.1 CHF₂ CHF₂ IA-482 A¹.1 CH₂Cl CHF₂ IA-483 A¹.1 CH₂CH₂CN CHF₂ IA-484 A¹.1 CH₂CH₂Cl CHF₂ IA-485 A¹.1 CH₂CH₂OH CHF₂ IA-486 A¹.1 CH₂CH₂CH₂OH CHF₂ IA-487 A¹.1 CH₂CH(OH)CH₂OH CHF₂ IA-488 A¹.1 CH₂CH(OCH₃)₂ CHF₂ IA-489 A¹.1 CH₂SCH₃ CHF₂ IA-490 A¹.1 (CH₂)₃SCH₃ CHF₂ IA-491 A¹.1 CH₂S(═O)CH₃ CHF₂ IA-492 A¹.1 CH₂S(═O)₂CH₃ CHF₂ IA-493 A¹.1 CH₂C(═O)CH₃ CHF₂ IA-494 A¹.1 CH₂C(═O)CH₂CH₃ CHF₂ IA-495 A¹.1 CH₂COOH CHF₂ IA-496 A¹.1 CH₂COOCH₃ CHF₂ IA-497 A¹.1 CH₂COOCH₂CH₃ CHF₂ IA-498 A¹.1 cyclo-C₃H₅ CHF₂ IA-499 A¹.1 cyclo-C₄H₇ CHF₂ IA-500 A¹.1 cyclo-C₅H₉ CHF₂ IA-501 A¹.1 cyclo-C₆H₁₁ CHF₂ IA-502 A¹.1 C₆H₅ CHF₂ IA-503 A¹.1 CH₂Cl CH₂Cl IA-504 A¹.1 CH₂CH₂CN CH₂Cl IA-505 A¹.1 CH₂CH₂Cl CH₂Cl IA-506 A¹.1 CH₂CH₂OH CH₂Cl IA-507 A¹.1 CH₂CH₂CH₂OH CH₂Cl IA-508 A¹.1 CH₂CH(OH)CH₂OH CH₂Cl IA-509 A¹.1 CH₂CH(OCH₃)₂ CH₂Cl IA-510 A¹.1 CH₂SCH₃ CH₂Cl IA-511 A¹.1 (CH₂)₃SCH₃ CH₂Cl IA-512 A¹.1 CH₂S(═O)CH₃ CH₂Cl IA-513 A¹.1 CH₂S(═O)₂CH₃ CH₂Cl IA-514 A¹.1 CH₂C(═O)CH₃ CH₂Cl IA-515 A¹.1 CH₂C(═O)CH₂CH₃ CH₂Cl IA-516 A¹.1 CH₂COOH CH₂Cl IA-517 A¹.1 CH₂COOCH₃ CH₂Cl IA-518 A¹.1 CH₂COOCH₂CH₃ CH₂Cl IA-519 A¹.1 cyclo-C₃H₅ CH₂Cl IA-520 A¹.1 cyclo-C₄H₇ CH₂Cl IA-521 A¹.1 cyclo-C₅H₉ CH₂Cl IA-522 A¹.1 cyclo-C₆H₁₁ CH₂Cl IA-523 A¹.1 C₆H₅ CH₂Cl IA-524 A¹.1 CH₂CH₂CN CH₂CH₂CN IA-525 A¹.1 CH₂CH₂Cl CH₂CH₂CN IA-526 A¹.1 CH₂CH₂OH CH₂CH₂CN IA-527 A¹.1 CH₂CH₂CH₂OH CH₂CH₂CN IA-528 A¹.1 CH₂CH(OH)CH₂OH CH₂CH₂CN IA-529 A¹.1 CH₂CH(OCH₃)₂ CH₂CH₂CN IA-530 A¹.1 CH₂SCH₃ CH₂CH₂CN IA-531 A¹.1 (CH₂)₃SCH₃ CH₂CH₂CN IA-532 A¹.1 CH₂S(═O)CH₃ CH₂CH₂CN IA-533 A¹.1 CH₂S(═O)₂CH₃ CH₂CH₂CN IA-534 A¹.1 CH₂C(═O)CH₃ CH₂CH₂CN IA-535 A¹.1 CH₂C(═O)CH₂CH₃ CH₂CH₂CN IA-536 A¹.1 CH₂COOH CH₂CH₂CN IA-537 A¹.1 CH₂COOCH₃ CH₂CH₂CN IA-538 A¹.1 CH₂COOCH₂CH₃ CH₂CH₂CN IA-539 A¹.1 cyclo-C₃H₅ CH₂CH₂CN IA-540 A¹.1 cyclo-C₄H₇ CH₂CH₂CN IA-541 A¹.1 cyclo-C₅H₉ CH₂CH₂CN IA-542 A¹.1 cyclo-C₆H₁₁ CH₂CH₂CN IA-543 A¹.1 C₆H₅ CH₂CH₂CN IA-544 A¹.1 CH₂CH₂Cl CH₂CH₂Cl IA-545 A¹.1 CH₂CH₂OH CH₂CH₂Cl IA-546 A¹.1 CH₂CH₂CH₂OH CH₂CH₂Cl IA-547 A¹.1 CH₂CH(OH)CH₂OH CH₂CH₂Cl IA-548 A¹.1 CH₂CH(OCH₃)₂ CH₂CH₂Cl IA-549 A¹.1 CH₂SCH₃ CH₂CH₂Cl IA-550 A¹.1 (CH₂)₃SCH₃ CH₂CH₂Cl IA-551 A¹.1 CH₂S(═O)CH₃ CH₂CH₂Cl IA-552 A¹.1 CH₂S(═O)₂CH₃ CH₂CH₂Cl IA-553 A¹.1 CH₂C(═O)CH₃ CH₂CH₂Cl IA-554 A¹.1 CH₂C(═O)CH₂CH₃ CH₂CH₂Cl IA-555 A¹.1 CH₂COOH CH₂CH₂Cl IA-556 A¹.1 CH₂COOCH₃ CH₂CH₂Cl IA-557 A¹.1 CH₂COOCH₂CH₃ CH₂CH₂Cl IA-558 A¹.1 cyclo-C₃H₅ CH₂CH₂Cl IA-559 A¹.1 cyclo-C₄H₇ CH₂CH₂Cl IA-560 A¹.1 cyclo-C₅H₉ CH₂CH₂Cl IA-561 A¹.1 cyclo-C₆H₁₁ CH₂CH₂Cl IA-562 A¹.1 C₆H₅ CH₂CH₂Cl IA-563 A¹.1 CH₂CH₂OH CH₂CH₂OH IA-564 A¹.1 CH₂CH₂CH₂OH CH₂CH₂OH IA-565 A¹.1 CH₂CH(OH)CH₂OH CH₂CH₂OH IA-566 A¹.1 CH₂CH(OCH₃)₂ CH₂CH₂OH IA-567 A¹.1 CH₂SCH₃ CH₂CH₂OH IA-568 A¹.1 (CH₂)₃SCH₃ CH₂CH₂OH IA-569 A¹.1 CH₂S(═O)CH₃ CH₂CH₂OH IA-570 A¹.1 CH₂S(═O)₂CH₃ CH₂CH₂OH IA-571 A¹.1 CH₂C(═O)CH₃ CH₂CH₂OH IA-572 A¹.1 CH₂C(═O)CH₂CH₃ CH₂CH₂OH IA-573 A¹.1 CH₂COOH CH₂CH₂OH IA-574 A¹.1 CH₂COOCH₃ CH₂CH₂OH IA-575 A¹.1 CH₂COOCH₂CH₃ CH₂CH₂OH IA-576 A¹.1 cyclo-C₃H₅ CH₂CH₂OH IA-577 A¹.1 cyclo-C₄H₇ CH₂CH₂OH IA-578 A¹.1 cyclo-C₅H₉ CH₂CH₂OH IA-579 A¹.1 cyclo-C₆H₁₁ CH₂CH₂OH IA-580 A¹.1 C₆H₅ CH₂CH₂OH IA-581 A¹.1 CH₂CH₂CH₂OH CH₂CH₂CH₂OH IA-582 A¹.1 CH₂CH(OH)CH₂OH CH₂CH₂CH₂OH IA-583 A¹.1 CH₂CH(OCH₃)₂ CH₂CH₂CH₂OH IA-584 A¹.1 CH₂SCH₃ CH₂CH₂CH₂OH IA-585 A¹.1 (CH₂)₃SCH₃ CH₂CH₂CH₂OH IA-586 A¹.1 CH₂S(═O)CH₃ CH₂CH₂CH₂OH IA-587 A¹.1 CH₂S(═O)₂CH₃ CH₂CH₂CH₂OH IA-588 A¹.1 CH₂C(═O)CH₃ CH₂CH₂CH₂OH IA-589 A¹.1 CH₂C(═O)CH₂CH₃ CH₂CH₂CH₂OH IA-590 A¹.1 CH₂COOH CH₂CH₂CH₂OH IA-591 A¹.1 CH₂COOCH₃ CH₂CH₂CH₂OH IA-592 A¹.1 CH₂COOCH₂CH₃ CH₂CH₂CH₂OH IA-593 A¹.1 cyclo-C₃H₅ CH₂CH₂CH₂OH IA-594 A¹.1 cyclo-C₄H₇ CH₂CH₂CH₂OH IA-595 A¹.1 cyclo-C₅H₉ CH₂CH₂CH₂OH IA-596 A¹.1 cyclo-C₆H₁₁ CH₂CH₂CH₂OH IA-597 A¹.1 C₆H₅ CH₂CH₂CH₂OH IA-598 A¹.1 CH₂CH(OH)CH₂OH CH₂CH(OH)CH₂OH IA-599 A¹.1 CH₂CH(OCH₃)₂ CH₂CH(OH)CH₂OH IA-600 A¹.1 CH₂SCH₃ CH₂CH(OH)CH₂OH IA-601 A¹.1 (CH₂)₃SCH₃ CH₂CH(OH)CH₂OH IA-602 A¹.1 CH₂S(═O)CH₃ CH₂CH(OH)CH₂OH IA-603 A¹.1 CH₂S(═O)₂CH₃ CH₂CH(OH)CH₂OH IA-604 A¹.1 CH₂C(═O)CH₃ CH₂CH(OH)CH₂OH IA-605 A¹.1 CH₂C(═O)CH₂CH₃ CH₂CH(OH)CH₂OH IA-606 A¹.1 CH₂COOH CH₂CH(OH)CH₂OH IA-607 A¹.1 CH₂COOCH₃ CH₂CH(OH)CH₂OH IA-608 A¹.1 CH₂COOCH₂CH₃ CH₂CH(OH)CH₂OH IA-609 A¹.1 cyclo-C₃H₅ CH₂CH(OH)CH₂OH IA-610 A¹.1 cyclo-C₄H₇ CH₂CH(OH)CH₂OH IA-611 A¹.1 cyclo-C₅H₉ CH₂CH(OH)CH₂OH IA-612 A¹.1 cyclo-C₆H₁₁ CH₂CH(OH)CH₂OH IA-613 A¹.1 C₆H₅ CH₂CH(OH)CH₂OH IA-614 A¹.1 CH₂CH(OCH₃)₂ CH₂CH(OCH₃)₂ IA-615 A¹.1 CH₂SCH₃ CH₂CH(OCH₃)₂ IA-616 A¹.1 (CH₂)₃SCH₃ CH₂CH(OCH₃)₂ IA-617 A¹.1 CH₂S(═O)CH₃ CH₂CH(OCH₃)₂ IA-618 A¹.1 CH₂S(═O)₂CH₃ CH₂CH(OCH₃)₂ IA-619 A¹.1 CH₂C(═O)CH₃ CH₂CH(OCH₃)₂ IA-620 A¹.1 CH₂C(═O)CH₂CH₃ CH₂CH(OCH₃)₂ IA-621 A¹.1 CH₂COOH CH₂CH(OCH₃)₂ IA-622 A¹.1 CH₂COOCH₃ CH₂CH(OCH₃)₂ IA-623 A¹.1 CH₂COOCH₂CH₃ CH₂CH(OCH₃)₂ IA-624 A¹.1 cyclo-C₃H₅ CH₂CH(OCH₃)₂ IA-625 A¹.1 cyclo-C₄H₇ CH₂CH(OCH₃)₂ IA-626 A¹.1 cyclo-C₅H₉ CH₂CH(OCH₃)₂ IA-627 A¹.1 cyclo-C₆H₁₁ CH₂CH(OCH₃)₂ IA-628 A¹.1 C₆H₅ CH₂CH(OCH₃)₂ IA-629 A¹.1 CH₂SCH₃ CH₂SCH₃ IA-630 A¹.1 (CH₂)₃SCH₃ CH₂SCH₃ IA-631 A¹.1 CH₂S(═O)CH₃ CH₂SCH₃ IA-632 A¹.1 CH₂S(═O)₂CH₃ CH₂SCH₃ IA-633 A¹.1 CH₂C(═O)CH₃ CH₂SCH₃ IA-634 A¹.1 CH₂C(═O)CH₂CH₃ CH₂SCH₃ IA-635 A¹.1 CH₂COOH CH₂SCH₃ IA-636 A¹.1 CH₂COOCH₃ CH₂SCH₃ IA-637 A¹.1 CH₂COOCH₂CH₃ CH₂SCH₃ IA-638 A¹.1 cyclo-C₃H₅ CH₂SCH₃ IA-639 A¹.1 cyclo-C₄H₇ CH₂SCH₃ IA-640 A¹.1 cyclo-C₅H₉ CH₂SCH₃ IA-641 A¹.1 cyclo-C₆H₁₁ CH₂SCH₃ IA-642 A¹.1 C₆H₅ CH₂SCH₃ IA-643 A¹.1 (CH₂)₃SCH₃ (CH₂)₃SCH₃ IA-644 A¹.1 CH₂S(═O)CH₃ (CH₂)₃SCH₃ IA-645 A¹.1 CH₂S(═O)₂CH₃ (CH₂)₃SCH₃ IA-646 A¹.1 CH₂C(═O)CH₃ (CH₂)₃SCH₃ IA-647 A¹.1 CH₂C(═O)CH₂CH₃ (CH₂)₃SCH₃ IA-648 A¹.1 CH₂COOH (CH₂)₃SCH₃ IA-649 A¹.1 CH₂COOCH₃ (CH₂)₃SCH₃ IA-650 A¹.1 CH₂COOCH₂CH₃ (CH₂)₃SCH₃ IA-651 A¹.1 cyclo-C₃H₅ (CH₂)₃SCH₃ IA-652 A¹.1 cyclo-C₄H₇ (CH₂)₃SCH₃ IA-653 A¹.1 cyclo-C₅H₉ (CH₂)₃SCH₃ IA-654 A¹.1 cyclo-C₆H₁₁ (CH₂)₃SCH₃ IA-655 A¹.1 C₆H₅ (CH₂)₃SCH₃ IA-656 A¹.1 CH₂S(═O)CH₃ CH₂S(═O)CH₃ IA-657 A¹.1 CH₂S(═O)₂CH₃ CH₂S(═O)CH₃ IA-658 A¹.1 CH₂C(═O)CH₃ CH₂S(═O)CH₃ IA-659 A¹.1 CH₂C(═O)CH₂CH₃ CH₂S(═O)CH₃ IA-660 A¹.1 CH₂COOH CH₂S(═O)CH₃ IA-661 A¹.1 CH₂COOCH₃ CH₂S(═O)CH₃ IA-662 A¹.1 CH₂COOCH₂CH₃ CH₂S(═O)CH₃ IA-663 A¹.1 cyclo-C₃H₅ CH₂S(═O)CH₃ IA-664 A¹.1 cyclo-C₄H₇ CH₂S(═O)CH₃ IA-665 A¹.1 cyclo-C₅H₉ CH₂S(═O)CH₃ IA-666 A¹.1 cyclo-C₆H₁₁ CH₂S(═O)CH₃ IA-667 A¹.1 C₆H₅ CH₂S(═O)CH₃ IA-668 A¹.1 CH₂S(═O)₂CH₃ CH₂S(═O)₂CH₃ IA-669 A¹.1 CH₂C(═O)CH₃ CH₂S(═O)₂CH₃ IA-670 A¹.1 CH₂C(═O)CH₂CH₃ CH₂S(═O)₂CH₃ IA-671 A¹.1 CH₂COOH CH₂S(═O)₂CH₃ IA-672 A¹.1 CH₂COOCH₃ CH₂S(═O)₂CH₃ IA-673 A¹.1 CH₂COOCH₂CH₃ CH₂S(═O)₂CH₃ IA-674 A¹.1 cyclo-C₃H₅ CH₂S(═O)₂CH₃ IA-675 A¹.1 cyclo-C₄H₇ CH₂S(═O)₂CH₃ IA-676 A¹.1 cyclo-C₅H₉ CH₂S(═O)₂CH₃ IA-677 A¹.1 cyclo-C₆H₁₁ CH₂S(═O)₂CH₃ IA-678 A¹.1 C₆H₅ CH₂S(═O)₂CH₃ IA-679 A¹.1 CH₂C(═O)CH₃ CH₂C(═O)CH₃ IA-680 A¹.1 CH₂C(═O)CH₂CH₃ CH₂C(═O)CH₃ IA-681 A¹.1 CH₂COOH CH₂C(═O)CH₃ IA-682 A¹.1 CH₂COOCH₃ CH₂C(═O)CH₃ IA-683 A¹.1 CH₂COOCH₂CH₃ CH₂C(═O)CH₃ IA-684 A¹.1 cyclo-C₃H₅ CH₂C(═O)CH₃ IA-685 A¹.1 cyclo-C₄H₇ CH₂C(═O)CH₃ IA-686 A¹.1 cyclo-C₅H₉ CH₂C(═O)CH₃ IA-687 A¹.1 cyclo-C₆H₁₁ CH₂C(═O)CH₃ IA-688 A¹.1 C₆H₅ CH₂C(═O)CH₃ IA-689 A¹.1 CH₂C(═O)CH₂CH₃ CH₂C(═O)CH₂CH₃ IA-690 A¹.1 CH₂COOH CH₂C(═O)CH₂CH₃ IA-691 A¹.1 CH₂COOCH₃ CH₂C(═O)CH₂CH₃ IA-692 A¹.1 CH₂COOCH₂CH₃ CH₂C(═O)CH₂CH₃ IA-693 A¹.1 cyclo-C₃H₅ CH₂C(═O)CH₂CH₃ IA-694 A¹.1 cyclo-C₄H₇ CH₂C(═O)CH₂CH₃ IA-695 A¹.1 cyclo-C₅H₉ CH₂C(═O)CH₂CH₃ IA-696 A¹.1 cyclo-C₆H₁₁ CH₂C(═O)CH₂CH₃ IA-697 A¹.1 C₆H₅ CH₂C(═O)CH₂CH₃ IA-698 A¹.1 CH₂COOH CH₂COOH IA-699 A¹.1 CH₂COOCH₃ CH₂COOH IA-700 A¹.1 CH₂COOCH₂CH₃ CH₂COOH IA-701 A¹.1 cyclo-C₃H₅ CH₂COOH IA-702 A¹.1 cyclo-C₄H₇ CH₂COOH IA-703 A¹.1 cyclo-C₅H₉ CH₂COOH IA-704 A¹.1 cyclo-C₆H₁₁ CH₂COOH IA-705 A¹.1 C₆H₅ CH₂COOH IA-706 A¹.1 CH₂COOCH₃ CH₂COOCH₃ IA-707 A¹.1 CH₂COOCH₂CH₃ CH₂COOCH₃ IA-708 A¹.1 cyclo-C₃H₅ CH₂COOCH₃ IA-709 A¹.1 cyclo-C₄H₇ CH₂COOCH₃ IA-710 A¹.1 cyclo-C₅H₉ CH₂COOCH₃ IA-711 A¹.1 cyclo-C₆H₁₁ CH₂COOCH₃ IA-712 A¹.1 C₆H₅ CH₂COOCH₃ IA-713 A¹.1 CH₂COOCH₂CH₃ CH₂COOCH₂CH₃ IA-714 A¹.1 cyclo-C₃H₅ CH₂COOCH₂CH₃ IA-715 A¹.1 cyclo-C₄H₇ CH₂COOCH₂CH₃ IA-716 A¹.1 cyclo-C₅H₉ CH₂COOCH₂CH₃ IA-717 A¹.1 cyclo-C₆H₁₁ CH₂COOCH₂CH₃ IA-718 A¹.1 C₆H₅ CH₂COOCH₂CH₃ IA-719 A¹.1 cyclo-C₃H₅ cyclo-C₃H₅ IA-720 A¹.1 cyclo-C₄H₇ cyclo-C₃H₅ IA-721 A¹.1 cyclo-C₅H₉ cyclo-C₃H₅ IA-722 A¹.1 cyclo-C₆H₁₁ cyclo-C₃H₅ IA-723 A¹.1 C₆H₅ cyclo-C₃H₅ IA-724 A¹.1 cyclo-C₄H₇ cyclo-C₄H₇ IA-725 A¹.1 cyclo-C₅H₉ cyclo-C₄H₇ IA-726 A¹.1 cyclo-C₆H₁₁ cyclo-C₄H₇ IA-727 A¹.1 C₆H₅ cyclo-C₄H₇ IA-728 A¹.1 cyclo-C₅H₉ cyclo-C₅H₉ IA-729 A¹.1 cyclo-C₆H₁₁ cyclo-C₅H₉ IA-730 A¹.1 C₆H₅ cyclo-C₅H₉ IA-731 A¹.1 cyclo-C₆H₁₁ cyclo-C₆H₁₁ IA-732 A¹.1 C₆H₅ cyclo-C₆H₁₁ IA-733 A¹.1 C₆H₅ C₆H₅ IA-734

CH₃ CH₃ IA-735 A¹.2 CH₂CH₃ CH₃ IA-736 A¹.2 CH═CH₂ CH₃ IA-737 A¹.2 CH₂CH₂CH₃ CH₃ IA-738 A¹.2 CH(CH₃)₂ CH₃ IA-739 A¹.2 CH₂CH₂CH₂CH₃ CH₃ IA-740 A¹.2 C(CH₃)₃ CH₃ IA-741 A¹.2 CH₂CH(CH₃)₂ CH₃ IA-742 A¹.2 CH(CH₃)CH₂CH₃ CH₃ IA-743 A¹.2 CH₂CHCH₂ CH₃ IA-744 A¹.2 CH₂CCH CH₃ IA-745 A¹.2 CH(CH₃)CH═CH₂ CH₃ IA-746 A¹.2 CHF₂ CH₃ IA-747 A¹.2 CH₂Cl CH₃ IA-748 A¹.2 CH₂CH₂CN CH₃ IA-749 A¹.2 CH₂CH₂Cl CH₃ IA-750 A¹.2 CH₂CH₂OH CH₃ IA-751 A¹.2 CH₂CH₂CH₂OH CH₃ IA-752 A¹.2 CH₂CH(OH)CH₂OH CH₃ IA-753 A¹.2 CH₂CH(OCH₃)₂ CH₃ IA-754 A¹.2 CH₂SCH₃ CH₃ IA-755 A¹.2 (CH₂)₃SCH₃ CH₃ IA-756 A¹.2 CH₂S(═O)CH₃ CH₃ IA-757 A¹.2 CH₂S(═O)₂CH₃ CH₃ IA-758 A¹.2 CH₂C(═O)CH₃ CH₃ IA-759 A¹.2 CH₂C(═O)CH₂CH₃ CH₃ IA-760 A¹.2 CH₂COOH CH₃ IA-761 A¹.2 CH₂COOCH₃ CH₃ IA-762 A¹.2 CH₂COOCH₂CH₃ CH₃ IA-763 A¹.2 cyclo-C₃H₅ CH₃ IA-764 A¹.2 cyclo-C₄H₇ CH₃ IA-765 A¹.2 cyclo-C₅H₉ CH₃ IA-766 A¹.2 cyclo-C₆H₁₁ CH₃ IA-767 A¹.2 C₆H₅ CH₃ IA-768 A¹.2 CH₂CH₃ CH₂CH₃ IA-769 A¹.2 CH═CH₂ CH₂CH₃ IA-770 A¹.2 CH₂CH₂CH₃ CH₂CH₃ IA-771 A¹.2 CH(CH₃)₂ CH₂CH₃ IA-772 A¹.2 CH₂CH₂CH₂CH₃ CH₂CH₃ IA-773 A¹.2 C(CH₃)₃ CH₂CH₃ IA-774 A¹.2 CH₂CH(CH₃)₂ CH₂CH₃ IA-775 A¹.2 CH(CH₃)CH₂CH₃ CH₂CH₃ IA-776 A¹.2 CH₂CHCH₂ CH₂CH₃ IA-777 A¹.2 CH₂CCH CH₂CH₃ IA-778 A¹.2 CH(CH₃)CH═CH₂ CH₂CH₃ IA-779 A¹.2 CHF₂ CH₂CH₃ IA-780 A¹.2 CH₂Cl CH₂CH₃ IA-781 A¹.2 CH₂CH₂CN CH₂CH₃ IA-782 A¹.2 CH₂CH₂Cl CH₂CH₃ IA-783 A¹.2 CH₂CH₂OH CH₂CH₃ IA-784 A¹.2 CH₂CH₂CH₂OH CH₂CH₃ IA-785 A¹.2 CH₂CH(OH)CH₂OH CH₂CH₃ IA-786 A¹.2 CH₂CH(OCH₃)₂ CH₂CH₃ IA-787 A¹.2 CH₂SCH₃ CH₂CH₃ IA-788 A¹.2 (CH₂)₃SCH₃ CH₂CH₃ IA-789 A¹.2 CH₂S(═O)CH₃ CH₂CH₃ IA-790 A¹.2 CH₂S(═O)₂CH₃ CH₂CH₃ IA-791 A¹.2 CH₂C(═O)CH₃ CH₂CH₃ IA-792 A¹.2 CH₂C(═O)CH₂CH₃ CH₂CH₃ IA-793 A¹.2 CH₂COOH CH₂CH₃ IA-794 A¹.2 CH₂COOCH₃ CH₂CH₃ IA-795 A¹.2 CH₂COOCH₂CH₃ CH₂CH₃ IA-796 A¹.2 cyclo-C₃H₅ CH₂CH₃ IA-797 A¹.2 cyclo-C₄H₇ CH₂CH₃ IA-798 A¹.2 cyclo-C₅H₉ CH₂CH₃ IA-799 A¹.2 cyclo-C₆H₁₁ CH₂CH₃ IA-800 A¹.2 C₆H₅ CH₂CH₃ IA-801 A¹.2 CH═CH₂ CH═CH₂ IA-802 A¹.2 CH₂CH₂CH₃ CH═CH₂ IA-803 A¹.2 CH(CH₃)₂ CH═CH₂ IA-804 A¹.2 CH₂CH₂CH₂CH₃ CH═CH₂ IA-805 A¹.2 C(CH₃)₃ CH═CH₂ IA-806 A¹.2 CH₂CH(CH₃)₂ CH═CH₂ IA-807 A¹.2 CH(CH₃)CH₂CH₃ CH═CH₂ IA-808 A¹.2 CH₂CHCH₂ CH═CH₂ IA-809 A¹.2 CH₂CCH CH═CH₂ IA-810 A¹.2 CH(CH₃)CH═CH₂ CH═CH₂ IA-811 A¹.2 CHF₂ CH═CH₂ IA-812 A¹.2 CH₂Cl CH═CH₂ IA-813 A¹.2 CH₂CH₂CN CH═CH₂ IA-814 A¹.2 CH₂CH₂Cl CH═CH₂ IA-815 A¹.2 CH₂CH₂OH CH═CH₂ IA-816 A¹.2 CH₂CH₂CH₂OH CH═CH₂ IA-817 A¹.2 CH₂CH(OH)CH₂OH CH═CH₂ IA-818 A¹.2 CH₂CH(OCH₃)₂ CH═CH₂ IA-819 A¹.2 CH₂SCH₃ CH═CH₂ IA-820 A¹.2 (CH₂)₃SCH₃ CH═CH₂ IA-821 A¹.2 CH₂S(═O)CH₃ CH═CH₂ IA-822 A¹.2 CH₂S(═O)₂CH₃ CH═CH₂ IA-823 A¹.2 CH₂C(═O)CH₃ CH═CH₂ IA-824 A¹.2 CH₂C(═O)CH₂CH₃ CH═CH₂ IA-825 A¹.2 CH₂COOH CH═CH₂ IA-826 A¹.2 CH₂COOCH₃ CH═CH₂ IA-827 A¹.2 CH₂COOCH₂CH₃ CH═CH₂ IA-828 A¹.2 cyclo-C₃H₅ CH═CH₂ IA-829 A¹.2 cyclo-C₄H₇ CH═CH₂ IA-830 A¹.2 cyclo-C₅H₉ CH═CH₂ IA-831 A¹.2 cyclo-C₆H₁₁ CH═CH₂ IA-832 A¹.2 C₆H₅ CH═CH₂ IA-833 A¹.2 CH₂CH₂CH₃ CH₂CH₂CH₃ IA-834 A¹.2 CH(CH₃)₂ CH₂CH₂CH₃ IA-835 A¹.2 CH₂CH₂CH₂CH₃ CH₂CH₂CH₃ IA-836 A¹.2 C(CH₃)₃ CH₂CH₂CH₃ IA-837 A¹.2 CH₂CH(CH₃)₂ CH₂CH₂CH₃ IA-838 A¹.2 CH(CH₃)CH₂CH₃ CH₂CH₂CH₃ IA-839 A¹.2 CH₂CHCH₂ CH₂CH₂CH₃ IA-840 A¹.2 CH₂CCH CH₂CH₂CH₃ IA-841 A¹.2 CH(CH₃)CH═CH₂ CH₂CH₂CH₃ IA-842 A¹.2 CHF₂ CH₂CH₂CH₃ IA-843 A¹.2 CH₂Cl CH₂CH₂CH₃ IA-844 A¹.2 CH₂CH₂CN CH₂CH₂CH₃ IA-845 A¹.2 CH₂CH₂Cl CH₂CH₂CH₃ IA-846 A¹.2 CH₂CH₂OH CH₂CH₂CH₃ IA-847 A¹.2 CH₂CH₂CH₂OH CH₂CH₂CH₃ IA-848 A¹.2 CH₂CH(OH)CH₂OH CH₂CH₂CH₃ IA-849 A¹.2 CH₂CH(OCH₃)₂ CH₂CH₂CH₃ IA-850 A¹.2 CH₂SCH₃ CH₂CH₂CH₃ IA-851 A¹.2 (CH₂)₃SCH₃ CH₂CH₂CH₃ IA-852 A¹.2 CH₂S(═O)CH₃ CH₂CH₂CH₃ IA-853 A¹.2 CH₂S(═O)₂CH₃ CH₂CH₂CH₃ IA-854 A¹.2 CH₂C(═O)CH₃ CH₂CH₂CH₃ IA-855 A¹.2 CH₂C(═O)CH₂CH₃ CH₂CH₂CH₃ IA-856 A¹.2 CH₂COOH CH₂CH₂CH₃ IA-857 A¹.2 CH₂COOCH₃ CH₂CH₂CH₃ IA-858 A¹.2 CH₂COOCH₂CH₃ CH₂CH₂CH₃ IA-859 A¹.2 cyclo-C₃H₅ CH₂CH₂CH₃ IA-860 A¹.2 cyclo-C₄H₇ CH₂CH₂CH₃ IA-861 A¹.2 cyclo-C₅H₉ CH₂CH₂CH₃ IA-862 A¹.2 cyclo-C₆H₁₁ CH₂CH₂CH₃ IA-863 A¹.2 C₆H₅ CH₂CH₂CH₃ IA-864 A¹.2 CH(CH₃)₂ CH(CH₃)₂ IA-865 A¹.2 CH₂CH₂CH₂CH₃ CH(CH₃)₂ IA-866 A¹.2 C(CH₃)₃ CH(CH₃)₂ IA-867 A¹.2 CH₂CH(CH₃)₂ CH(CH₃)₂ IA-868 A¹.2 CH(CH₃)CH₂CH₃ CH(CH₃)₂ IA-869 A¹.2 CH₂CHCH₂ CH(CH₃)₂ IA-870 A¹.2 CH₂CCH CH(CH₃)₂ IA-871 A¹.2 CH(CH₃)CH═CH₂ CH(CH₃)₂ IA-872 A¹.2 CHF₂ CH(CH₃)₂ IA-873 A¹.2 CH₂Cl CH(CH₃)₂ IA-874 A¹.2 CH₂CH₂CN CH(CH₃)₂ IA-875 A¹.2 CH₂CH₂Cl CH(CH₃)₂ IA-876 A¹.2 CH₂CH₂OH CH(CH₃)₂ IA-877 A¹.2 CH₂CH₂CH₂OH CH(CH₃)₂ IA-878 A¹.2 CH₂CH(OH)CH₂OH CH(CH₃)₂ IA-879 A¹.2 CH₂CH(OCH₃)₂ CH(CH₃)₂ IA-880 A¹.2 CH₂SCH₃ CH(CH₃)₂ IA-881 A¹.2 (CH₂)₃SCH₃ CH(CH₃)₂ IA-882 A¹.2 CH₂S(═O)CH₃ CH(CH₃)₂ IA-883 A¹.2 CH₂S(═O)₂CH₃ CH(CH₃)₂ IA-884 A¹.2 CH₂C(═O)CH₃ CH(CH₃)₂ IA-885 A¹.2 CH₂C(═O)CH₂CH₃ CH(CH₃)₂ IA-886 A¹.2 CH₂COOH CH(CH₃)₂ IA-887 A¹.2 CH₂COOCH₃ CH(CH₃)₂ IA-888 A¹.2 CH₂COOCH₂CH₃ CH(CH₃)₂ IA-889 A¹.2 cyclo-C₃H₅ CH(CH₃)₂ IA-890 A¹.2 cyclo-C₄H₇ CH(CH₃)₂ IA-891 A¹.2 cyclo-C₅H₉ CH(CH₃)₂ IA-892 A¹.2 cyclo-C₆H₁₁ CH(CH₃)₂ IA-893 A¹.2 C₆H₅ CH(CH₃)₂ IA-894 A¹.2 CH₂CH₂CH₂CH₃ CH₂CH₂CH₂CH₃ IA-895 A¹.2 C(CH₃)₃ CH₂CH₂CH₂CH₃ IA-896 A¹.2 CH₂CH(CH₃)₂ CH₂CH₂CH₂CH₃ IA-897 A¹.2 CH(CH₃)CH₂CH₃ CH₂CH₂CH₂CH₃ IA-898 A¹.2 CH₂CHCH₂ CH₂CH₂CH₂CH₃ IA-899 A¹.2 CH₂CCH CH₂CH₂CH₂CH₃ IA-900 A¹.2 CH(CH₃)CH═CH₂ CH₂CH₂CH₂CH₃ IA-901 A¹.2 CHF₂ CH₂CH₂CH₂CH₃ IA-902 A¹.2 CH₂Cl CH₂CH₂CH₂CH₃ IA-903 A¹.2 CH₂CH₂CN CH₂CH₂CH₂CH₃ IA-904 A¹.2 CH₂CH₂Cl CH₂CH₂CH₂CH₃ IA-905 A¹.2 CH₂CH₂OH CH₂CH₂CH₂CH₃ IA-906 A¹.2 CH₂CH₂CH₂OH CH₂CH₂CH₂CH₃ IA-907 A¹.2 CH₂CH(OH)CH₂OH CH₂CH₂CH₂CH₃ IA-908 A¹.2 CH₂CH(OCH₃)₂ CH₂CH₂CH₂CH₃ IA-909 A¹.2 CH₂SCH₃ CH₂CH₂CH₂CH₃ IA-910 A¹.2 (CH₂)₃SCH₃ CH₂CH₂CH₂CH₃ IA-911 A¹.2 CH₂S(═O)CH₃ CH₂CH₂CH₂CH₃ IA-912 A¹.2 CH₂S(═O)₂CH₃ CH₂CH₂CH₂CH₃ IA-913 A¹.2 CH₂C(═O)CH₃ CH₂CH₂CH₂CH₃ IA-914 A¹.2 CH₂C(═O)CH₂CH₃ CH₂CH₂CH₂CH₃ IA-915 A¹.2 CH₂COOH CH₂CH₂CH₂CH₃ IA-916 A¹.2 CH₂COOCH₃ CH₂CH₂CH₂CH₃ IA-917 A¹.2 CH₂COOCH₂CH₃ CH₂CH₂CH₂CH₃ IA-918 A¹.2 cyclo-C₃H₅ CH₂CH₂CH₂CH₃ IA-919 A¹.2 cyclo-C₄H₇ CH₂CH₂CH₂CH₃ IA-920 A¹.2 cyclo-C₅H₉ CH₂CH₂CH₂CH₃ IA-921 A¹.2 cyclo-C₆H₁₁ CH₂CH₂CH₂CH₃ IA-922 A¹.2 C₆H₅ CH₂CH₂CH₂CH₃ IA-923 A¹.2 C(CH₃)₃ C(CH₃)₃ IA-924 A¹.2 CH₂CH(CH₃)₂ C(CH₃)₃ IA-925 A¹.2 CH(CH₃)CH₂CH₃ C(CH₃)₃ IA-926 A¹.2 CH₂CHCH₂ C(CH₃)₃ IA-927 A¹.2 CH₂CCH C(CH₃)₃ IA-928 A¹.2 CH(CH₃)CH═CH₂ C(CH₃)₃ IA-929 A¹.2 CHF₂ C(CH₃)₃ IA-930 A¹.2 CH₂Cl C(CH₃)₃ IA-931 A¹.2 CH₂CH₂CN C(CH₃)₃ IA-932 A¹.2 CH₂CH₂Cl C(CH₃)₃ IA-933 A¹.2 CH₂CH₂OH C(CH₃)₃ IA-934 A¹.2 CH₂CH₂CH₂OH C(CH₃)₃ IA-935 A¹.2 CH₂CH(OH)CH₂OH C(CH₃)₃ IA-936 A¹.2 CH₂CH(OCH₃)₂ C(CH₃)₃ IA-937 A¹.2 CH₂SCH₃ C(CH₃)₃ IA-938 A¹.2 (CH₂)₃SCH₃ C(CH₃)₃ IA-939 A¹.2 CH₂S(═O)CH₃ C(CH₃)₃ IA-940 A¹.2 CH₂S(═O)₂CH₃ C(CH₃)₃ IA-941 A¹.2 CH₂C(═O)CH₃ C(CH₃)₃ IA-942 A¹.2 CH₂C(═O)CH₂CH₃ C(CH₃)₃ IA-943 A¹.2 CH₂COOH C(CH₃)₃ IA-944 A¹.2 CH₂COOCH₃ C(CH₃)₃ IA-945 A¹.2 CH₂COOCH₂CH₃ C(CH₃)₃ IA-946 A¹.2 cyclo-C₃H₅ C(CH₃)₃ IA-947 A¹.2 cyclo-C₄H₇ C(CH₃)₃ IA-948 A¹.2 cyclo-C₅H₉ C(CH₃)₃ IA-949 A¹.2 cyclo-C₆H₁₁ C(CH₃)₃ IA-950 A¹.2 C₆H₅ C(CH₃)₃ IA-951 A¹.2 CH₂CH(CH₃)₂ CH₂CH(CH₃)₂ IA-952 A¹.2 CH(CH₃)CH₂CH₃ CH₂CH(CH₃)₂ IA-953 A¹.2 CH₂CHCH₂ CH₂CH(CH₃)₂ IA-954 A¹.2 CH₂CCH CH₂CH(CH₃)₂ IA-955 A¹.2 CH(CH₃)CH═CH₂ CH₂CH(CH₃)₂ IA-956 A¹.2 CHF₂ CH₂CH(CH₃)₂ IA-957 A¹.2 CH₂Cl CH₂CH(CH₃)₂ IA-958 A¹.2 CH₂CH₂CN CH₂CH(CH₃)₂ IA-959 A¹.2 CH₂CH₂Cl CH₂CH(CH₃)₂ IA-960 A¹.2 CH₂CH₂OH CH₂CH(CH₃)₂ IA-961 A¹.2 CH₂CH₂CH₂OH CH₂CH(CH₃)₂ IA-962 A¹.2 CH₂CH(OH)CH₂OH CH₂CH(CH₃)₂ IA-963 A¹.2 CH₂CH(OCH₃)₂ CH₂CH(CH₃)₂ IA-964 A¹.2 CH₂SCH₃ CH₂CH(CH₃)₂ IA-965 A¹.2 (CH₂)₃SCH₃ CH₂CH(CH₃)₂ IA-966 A¹.2 CH₂S(═O)CH₃ CH₂CH(CH₃)₂ IA-967 A¹.2 CH₂S(═O)₂CH₃ CH₂CH(CH₃)₂ IA-968 A¹.2 CH₂C(═O)CH₃ CH₂CH(CH₃)₂ IA-969 A¹.2 CH₂C(═O)CH₂CH₃ CH₂CH(CH₃)₂ IA-970 A¹.2 CH₂COOH CH₂CH(CH₃)₂ IA-971 A¹.2 CH₂COOCH₃ CH₂CH(CH₃)₂ IA-972 A¹.2 CH₂COOCH₂CH₃ CH₂CH(CH₃)₂ IA-973 A¹.2 cyclo-C₃H₅ CH₂CH(CH₃)₂ IA-974 A¹.2 cyclo-C₄H₇ CH₂CH(CH₃)₂ IA-975 A¹.2 cyclo-C₅H₉ CH₂CH(CH₃)₂ IA-976 A¹.2 cyclo-C₆H₁₁ CH₂CH(CH₃)₂ IA-977 A¹.2 C₆H₅ CH₂CH(CH₃)₂ IA-978 A¹.2 CH(CH₃)CH₂CH₃ CH(CH₃)CH₂CH₃ IA-979 A¹.2 CH₂CHCH₂ CH(CH₃)CH₂CH₃ IA-980 A¹.2 CH₂CCH CH(CH₃)CH₂CH₃ IA-981 A¹.2 CH(CH₃)CH═CH₂ CH(CH₃)CH₂CH₃ IA-982 A¹.2 CHF₂ CH(CH₃)CH₂CH₃ IA-983 A¹.2 CH₂Cl CH(CH₃)CH₂CH₃ IA-984 A¹.2 CH₂CH₂CN CH(CH₃)CH₂CH₃ IA-985 A¹.2 CH₂CH₂Cl CH(CH₃)CH₂CH₃ IA-986 A¹.2 CH₂CH₂OH CH(CH₃)CH₂CH₃ IA-987 A¹.2 CH₂CH₂CH₂OH CH(CH₃)CH₂CH₃ IA-988 A¹.2 CH₂CH(OH)CH₂OH CH(CH₃)CH₂CH₃ IA-989 A¹.2 CH₂CH(OCH₃)₂ CH(CH₃)CH₂CH₃ IA-990 A¹.2 CH₂SCH₃ CH(CH₃)CH₂CH₃ IA-991 A¹.2 (CH₂)₃SCH₃ CH(CH₃)CH₂CH₃ IA-992 A¹.2 CH₂S(═O)CH₃ CH(CH₃)CH₂CH₃ IA-993 A¹.2 CH₂S(═O)₂CH₃ CH(CH₃)CH₂CH₃ IA-994 A¹.2 CH₂C(═O)CH₃ CH(CH₃)CH₂CH₃ IA-995 A¹.2 CH₂C(═O)CH₂CH₃ CH(CH₃)CH₂CH₃ IA-996 A¹.2 CH₂COOH CH(CH₃)CH₂CH₃ IA-997 A¹.2 CH₂COOCH₃ CH(CH₃)CH₂CH₃ IA-998 A¹.2 CH₂COOCH₂CH₃ CH(CH₃)CH₂CH₃ IA-999 A¹.2 cyclo-C₃H₅ CH(CH₃)CH₂CH₃ IA-1000 A¹.2 cyclo-C₄H₇ CH(CH₃)CH₂CH₃ IA-1001 A¹.2 cyclo-C₅H₉ CH(CH₃)CH₂CH₃ IA-1002 A¹.2 cyclo-C₆H₁₁ CH(CH₃)CH₂CH₃ IA-1003 A¹.2 C₆H₅ CH(CH₃)CH₂CH₃ IA-1004 A¹.2 CH₂CHCH₂ CH₂CHCH₂ IA-1005 A¹.2 CH₂CCH CH₂CHCH₂ IA-1006 A¹.2 CH(CH₃)CH═CH₂ CH₂CHCH₂ IA-1007 A¹.2 CHF₂ CH₂CHCH₂ IA-1008 A¹.2 CH₂Cl CH₂CHCH₂ IA-1009 A¹.2 CH₂CH₂CN CH₂CHCH₂ IA-1010 A¹.2 CH₂CH₂Cl CH₂CHCH₂ IA-1011 A¹.2 CH₂CH₂OH CH₂CHCH₂ IA-1012 A¹.2 CH₂CH₂CH₂OH CH₂CHCH₂ IA-1013 A¹.2 CH₂CH(OH)CH₂OH CH₂CHCH₂ IA-1014 A¹.2 CH₂CH(OCH₃)₂ CH₂CHCH₂ IA-1015 A¹.2 CH₂SCH₃ CH₂CHCH₂ IA-1016 A¹.2 (CH₂)₃SCH₃ CH₂CHCH₂ IA-1017 A¹.2 CH₂S(═O)CH₃ CH₂CHCH₂ IA-1018 A¹.2 CH₂S(═O)₂CH₃ CH₂CHCH₂ IA-1019 A¹.2 CH₂C(═O)CH₃ CH₂CHCH₂ IA-1020 A¹.2 CH₂C(═O)CH₂CH₃ CH₂CHCH₂ IA-1021 A¹.2 CH₂COOH CH₂CHCH₂ IA-1022 A¹.2 CH₂COOCH₃ CH₂CHCH₂ IA-1023 A¹.2 CH₂COOCH₂CH₃ CH₂CHCH₂ IA-1024 A¹.2 cyclo-C₃H₅ CH₂CHCH₂ IA-1025 A¹.2 cyclo-C₄H₇ CH₂CHCH₂ IA-1026 A¹.2 cyclo-C₅H₉ CH₂CHCH₂ IA-1027 A¹.2 cyclo-C₆H₁₁ CH₂CHCH₂ IA-1028 A¹.2 C₆H₅ CH₂CHCH₂ IA-1029 A¹.2 CH₂CCH CH₂CCH IA-1030 A¹.2 CH(CH₃)CH═CH₂ CH₂CCH IA-1031 A¹.2 CHF₂ CH₂CCH IA-1032 A¹.2 CH₂Cl CH₂CCH IA-1033 A¹.2 CH₂CH₂CN CH₂CCH IA-1034 A¹.2 CH₂CH₂Cl CH₂CCH IA-1035 A¹.2 CH₂CH₂OH CH₂CCH IA-1036 A¹.2 CH₂CH₂CH₂OH CH₂CCH IA-1037 A¹.2 CH₂CH(OH)CH₂OH CH₂CCH IA-1038 A¹.2 CH₂CH(OCH₃)₂ CH₂CCH lA-1039 A¹.2 CH₂SCH₃ CH₂CCH IA-1040 A¹.2 (CH₂)₃SCH₃ CH₂CCH IA-1041 A¹.2 CH₂S(═O)CH₃ CH₂CCH IA-1042 A¹.2 CH₂S(═O)₂CH₃ CH₂CCH IA-1043 A¹.2 CH₂C(═O)CH₃ CH₂CCH IA-1044 A¹.2 CH₂C(═O)CH₂CH₃ CH₂CCH IA-1045 A¹.2 CH₂COOH CH₂CCH IA-1046 A¹.2 CH₂COOCH₃ CH₂CCH IA-1047 A¹.2 CH₂COOCH₂CH₃ CH₂CCH IA-1048 A¹.2 cyclo-C₃H₅ CH₂CCH IA-1049 A¹.2 cyclo-C₄H₇ CH₂CCH IA-1050 A¹.2 cyclo-C₅H₉ CH₂CCH IA-1051 A¹.2 cyclo-C₆H₁₁ CH₂CCH IA-1052 A¹.2 C₆H₅ CH₂CCH IA-1053 A¹.2 CH(CH₃)CH═CH₂ CH(CH₃)CH═CH₂ IA-1054 A¹.2 CHF₂ CH(CH₃)CH═CH₂ IA-1055 A¹.2 CH₂Cl CH(CH₃)CH═CH₂ IA-1056 A¹.2 CH₂CH₂CN CH(CH₃)CH═CH₂ IA-1057 A¹.2 CH₂CH₂Cl CH(CH₃)CH═CH₂ IA-1058 A¹.2 CH₂CH₂OH CH(CH₃)CH═CH₂ IA-1059 A¹.2 CH₂CH₂CH₂OH CH(CH₃)CH═CH₂ IA-1060 A¹.2 CH₂CH(OH)CH₂OH CH(CH₃)CH═CH₂ IA-1061 A¹.2 CH₂CH(OCH₃)₂ CH(CH₃)CH═CH₂ IA-1062 A¹.2 CH₂SCH₃ CH(CH₃)CH═CH₂ IA-1063 A¹.2 (CH₂)₃SCH₃ CH(CH₃)CH═CH₂ IA-1064 A¹.2 CH₂S(═O)CH₃ CH(CH₃)CH═CH₂ IA-1065 A¹.2 CH₂S(═O)₂CH₃ CH(CH₃)CH═CH₂ IA-1066 A¹.2 CH₂C(═O)CH₃ CH(CH₃)CH═CH₂ IA-1067 A¹.2 CH₂C(═O)CH₂CH₃ CH(CH₃)CH═CH₂ IA-1068 A¹.2 CH₂COOH CH(CH₃)CH═CH₂ IA-1069 A¹.2 CH₂COOCH₃ CH(CH₃)CH═CH₂ IA-1070 A¹.2 CH₂COOCH₂CH₃ CH(CH₃)CH═CH₂ IA-1071 A¹.2 cyclo-C₃H₅ CH(CH₃)CH═CH₂ IA-1072 A¹.2 cyclo-C₄H₇ CH(CH₃)CH═CH₂ IA-1073 A¹.2 cyclo-C₅H₉ CH(CH₃)CH═CH₂ IA-1074 A¹.2 cyclo-C₆H₁₁ CH(CH₃)CH═CH₂ IA-1075 A¹.2 C₆H₅ CH(CH₃)CH═CH₂ IA-1076 A¹.2 CHF₂ CHF₂ IA-1077 A¹.2 CH₂Cl CHF₂ IA-1078 A¹.2 CH₂CH₂CN CHF₂ IA-1079 A¹.2 CH₂CH₂Cl CHF₂ IA-1080 A¹.2 CH₂CH₂OH CHF₂ IA-1081 A¹.2 CH₂CH₂CH₂OH CHF₂ IA-1082 A¹.2 CH₂CH(OH)CH₂OH CHF₂ IA-1083 A¹.2 CH₂CH(OCH₃)₂ CHF₂ IA-1084 A¹.2 CH₂SCH₃ CHF₂ IA-1085 A¹.2 (CH₂)₃SCH₃ CHF₂ IA-1086 A¹.2 CH₂S(═O)CH₃ CHF₂ IA-1087 A¹.2 CH₂S(═O)₂CH₃ CHF₂ IA-1088 A¹.2 CH₂C(═O)CH₃ CHF₂ IA-1089 A¹.2 CH₂C(═O)CH₂CH₃ CHF₂ IA-1090 A¹.2 CH₂COOH CHF₂ IA-1091 A¹.2 CH₂COOCH₃ CHF₂ IA-1092 A¹.2 CH₂COOCH₂CH₃ CHF₂ IA-1093 A¹.2 cyclo-C₃H₅ CHF₂ IA-1094 A¹.2 cyclo-C₄H₇ CHF₂ IA-1095 A¹.2 cyclo-C₅H₉ CHF₂ IA-1096 A¹.2 cyclo-C₆H₁₁ CHF₂ IA-1097 A¹.2 C₆H₅ CHF₂ IA-1098 A¹.2 CH₂Cl CH₂Cl IA-1099 A¹.2 CH₂CH₂CN CH₂Cl IA-1100 A¹.2 CH₂CH₂Cl CH₂Cl IA-1101 A¹.2 CH₂CH₂OH CH₂Cl IA-1102 A¹.2 CH₂CH₂CH₂OH CH₂Cl IA-1103 A¹.2 CH₂CH(OH)CH₂OH CH₂Cl IA-1104 A¹.2 CH₂CH(OCH₃)₂ CH₂Cl IA-1105 A¹.2 CH₂SCH₃ CH₂Cl IA-1106 A¹.2 (CH₂)₃SCH₃ CH₂Cl IA-1107 A¹.2 CH₂S(═O)CH₃ CH₂Cl IA-1108 A¹.2 CH₂S(═O)₂CH₃ CH₂Cl IA-1109 A¹.2 CH₂C(═O)CH₃ CH₂Cl IA-1110 A¹.2 CH₂C(═O)CH₂CH₃ CH₂Cl IA-1111 A¹.2 CH₂COOH CH₂Cl IA-1112 A¹.2 CH₂COOCH₃ CH₂Cl IA-1113 A¹.2 CH₂COOCH₂CH₃ CH₂Cl IA-1114 A¹.2 cyclo-C₃H₅ CH₂Cl IA-1115 A¹.2 cyclo-C₄H₇ CH₂Cl IA-1116 A¹.2 cyclo-C₅H₉ CH₂Cl IA-1117 A¹.2 cyclo-C₆H₁₁ CH₂Cl IA-1118 A¹.2 C₆H₅ CH₂Cl IA-1119 A¹.2 CH₂CH₂CN CH₂CH₂CN IA-1120 A¹.2 CH₂CH₂Cl CH₂CH₂CN IA-1121 A¹.2 CH₂CH₂OH CH₂CH₂CN IA-1122 A¹.2 CH₂CH₂CH₂OH CH₂CH₂CN IA-1123 A¹.2 CH₂CH(OH)CH₂OH CH₂CH₂CN IA-1124 A¹.2 CH₂CH(OCH₃)₂ CH₂CH₂CN IA-1125 A¹.2 CH₂SCH₃ CH₂CH₂CN IA-1126 A¹.2 (CH₂)₃SCH₃ CH₂CH₂CN IA-1127 A¹.2 CH₂S(═O)CH₃ CH₂CH₂CN IA-1128 A¹.2 CH₂S(═O)₂CH₃ CH₂CH₂CN IA-1129 A¹.2 CH₂C(═O)CH₃ CH₂CH₂CN IA-1130 A¹.2 CH₂C(═O)CH₂CH₃ CH₂CH₂CN IA-1131 A¹.2 CH₂COOH CH₂CH₂CN IA-1132 A¹.2 CH₂COOCH₃ CH₂CH₂CN IA-1133 A¹.2 CH₂COOCH₂CH₃ CH₂CH₂CN IA-1134 A¹.2 cyclo-C₃H₅ CH₂CH₂CN IA-1135 A¹.2 cyclo-C₄H₇ CH₂CH₂CN IA-1136 A¹.2 cyclo-C₅H₉ CH₂CH₂CN IA-1137 A¹.2 cyclo-C₆H₁₁ CH₂CH₂CN IA-1138 A¹.2 C₆H₅ CH₂CH₂CN IA-1139 A¹.2 CH₂CH₂Cl CH₂CH₂Cl IA-1140 A¹.2 CH₂CH₂OH CH₂CH₂Cl IA-1141 A¹.2 CH₂CH₂CH₂OH CH₂CH₂Cl IA-1142 A¹.2 CH₂CH(OH)CH₂OH CH₂CH₂Cl IA-1143 A¹.2 CH₂CH(OCH₃)₂ CH₂CH₂Cl IA-1144 A¹.2 CH₂SCH₃ CH₂CH₂Cl IA-1145 A¹.2 (CH₂)₃SCH₃ CH₂CH₂Cl IA-1146 A¹.2 CH₂S(═O)CH₃ CH₂CH₂Cl IA-1147 A¹.2 CH₂S(═O)₂CH₃ CH₂CH₂Cl IA-1148 A¹.2 CH₂C(═O)CH₃ CH₂CH₂Cl IA-1149 A¹.2 CH₂C(═O)CH₂CH₃ CH₂CH₂Cl IA-1150 A¹.2 CH₂COOH CH₂CH₂Cl IA-1151 A¹.2 CH₂COOCH₃ CH₂CH₂Cl IA-1152 A¹.2 CH₂COOCH₂CH₃ CH₂CH₂Cl IA-1153 A¹.2 cyclo-C₃H₅ CH₂CH₂Cl IA-1154 A¹.2 cyclo-C₄H₇ CH₂CH₂Cl IA-1155 A¹.2 cyclo-C₅H₉ CH₂CH₂Cl IA-1156 A¹.2 cyclo-C₆H₁₁ CH₂CH₂Cl IA-1157 A¹.2 C₆H₅ CH₂CH₂Cl IA-1158 A¹.2 CH₂CH₂OH CH₂CH₂OH IA-1159 A¹.2 CH₂CH₂CH₂OH CH₂CH₂OH IA-1160 A¹.2 CH₂CH(OH)CH₂OH CH₂CH₂OH IA-1161 A¹.2 CH₂CH(OCH₃)₂ CH₂CH₂OH IA-1162 A¹.2 CH₂SCH₃ CH₂CH₂OH IA-1163 A¹.2 (CH₂)₃SCH₃ CH₂CH₂OH IA-1164 A¹.2 CH₂S(═O)CH₃ CH₂CH₂OH IA-1165 A¹.2 CH₂S(═O)₂CH₃ CH₂CH₂OH IA-1166 A¹.2 CH₂C(═O)CH₃ CH₂CH₂OH IA-1167 A¹.2 CH₂C(═O)CH₂CH₃ CH₂CH₂OH IA-1168 A¹.2 CH₂COOH CH₂CH₂OH IA-1169 A¹.2 CH₂COOCH₃ CH₂CH₂OH IA-1170 A¹.2 CH₂COOCH₂CH₃ CH₂CH₂OH IA-1171 A¹.2 cyclo-C₃H₅ CH₂CH₂OH IA-1172 A¹.2 cyclo-C₄H₇ CH₂CH₂OH IA-1173 A¹.2 cyclo-C₅H₉ CH₂CH₂OH IA-1174 A¹.2 cyclo-C₆H₁₁ CH₂CH₂OH IA-1175 A¹.2 C₆H₅ CH₂CH₂OH IA-1176 A¹.2 CH₂CH₂CH₂OH CH₂CH₂CH₂OH IA-1177 A¹.2 CH₂CH(OH)CH₂OH CH₂CH₂CH₂OH IA-1178 A¹.2 CH₂CH(OCH₃)₂ CH₂CH₂CH₂OH IA-1179 A¹.2 CH₂SCH₃ CH₂CH₂CH₂OH IA-1180 A¹.2 (CH₂)₃SCH₃ CH₂CH₂CH₂OH IA-1181 A¹.2 CH₂S(═O)CH₃ CH₂CH₂CH₂OH IA-1182 A¹.2 CH₂S(═O)₂CH₃ CH₂CH₂CH₂OH IA-1183 A¹.2 CH₂C(═O)CH₃ CH₂CH₂CH₂OH IA-1184 A¹.2 CH₂C(═O)CH₂CH₃ CH₂CH₂CH₂OH IA-1185 A¹.2 CH₂COOH CH₂CH₂CH₂OH IA-1186 A¹.2 CH₂COOCH₃ CH₂CH₂CH₂OH IA-1187 A¹.2 CH₂COOCH₂CH₃ CH₂CH₂CH₂OH IA-1188 A¹.2 cyclo-C₃H₅ CH₂CH₂CH₂OH IA-1189 A¹.2 cyclo-C₄H₇ CH₂CH₂CH₂OH IA-1190 A¹.2 cyclo-C₅H₉ CH₂CH₂CH₂OH IA-1191 A¹.2 cyclo-C₆H₁₁ CH₂CH₂CH₂OH IA-1192 A¹.2 C₆H₅ CH₂CH₂CH₂OH IA-1193 A¹.2 CH₂CH(OH)CH₂OH CH₂CH(OH)CH₂OH IA-1194 A¹.2 CH₂CH(OCH₃)₂ CH₂CH(OH)CH₂OH IA-1195 A¹.2 CH₂SCH₃ CH₂CH(OH)CH₂OH IA-1196 A¹.2 (CH₂)₃SCH₃ CH₂CH(OH)CH₂OH IA-1197 A¹.2 CH₂S(═O)CH₃ CH₂CH(OH)CH₂OH IA-1198 A¹.2 CH₂S(═O)₂CH₃ CH₂CH(OH)CH₂OH IA-1199 A¹.2 CH₂C(═O)CH₃ CH₂CH(OH)CH₂OH IA-1200 A¹.2 CH₂C(═O)CH₂CH₃ CH₂CH(OH)CH₂OH IA-1201 A¹.2 CH₂COOH CH₂CH(OH)CH₂OH IA-1202 A¹.2 CH₂COOCH₃ CH₂CH(OH)CH₂OH IA-1203 A¹.2 CH₂COOCH₂CH₃ CH₂CH(OH)CH₂OH IA-1204 A¹.2 cyclo-C₃H₅ CH₂CH(OH)CH₂OH IA-1205 A¹.2 cyclo-C₄H₇ CH₂CH(OH)CH₂OH IA-1206 A¹.2 cyclo-C₅H₉ CH₂CH(OH)CH₂OH IA-1207 A¹.2 cyclo-C₆H₁₁ CH₂CH(OH)CH₂OH IA-1208 A¹.2 C₆H₅ CH₂CH(OH)CH₂OH IA-1209 A¹.2 CH₂CH(OCH₃)₂ CH₂CH(OCH₃)₂ IA-1210 A¹.2 CH₂SCH₃ CH₂CH(OCH₃)₂ IA-1211 A¹.2 (CH₂)₃SCH₃ CH₂CH(OCH₃)₂ IA-1212 A¹.2 CH₂S(═O)CH₃ CH₂CH(OCH₃)₂ IA-1213 A¹.2 CH₂S(═O)₂CH₃ CH₂CH(OCH₃)₂ IA-1214 A¹.2 CH₂C(═O)CH₃ CH₂CH(OCH₃)₂ IA-1215 A¹.2 CH₂C(═O)CH₂CH₃ CH₂CH(OCH₃)₂ IA-1216 A¹.2 CH₂COOH CH₂CH(OCH₃)₂ IA-1217 A¹.2 CH₂COOCH₃ CH₂CH(OCH₃)₂ IA-1218 A¹.2 CH₂COOCH₂CH₃ CH₂CH(OCH₃)₂ IA-1219 A¹.2 cyclo-C₃H₅ CH₂CH(OCH₃)₂ IA-1220 A¹.2 cyclo-C₄H₇ CH₂CH(OCH₃)₂ IA-1221 A¹.2 cyclo-C₅H₉ CH₂CH(OCH₃)₂ IA-1222 A¹.2 cyclo-C₆H₁₁ CH₂CH(OCH₃)₂ IA-1223 A¹.2 C₆H₅ CH₂CH(OCH₃)₂ IA-1224 A¹.2 CH₂SCH₃ CH₂SCH₃ IA-1225 A¹.2 (CH₂)₃SCH₃ CH₂SCH₃ IA-1226 A¹.2 CH₂S(═O)CH₃ CH₂SCH₃ IA-1227 A¹.2 CH₂S(═O)₂CH₃ CH₂SCH₃ IA-1228 A¹.2 CH₂C(═O)CH₃ CH₂SCH₃ IA-1229 A¹.2 CH₂C(═O)CH₂CH₃ CH₂SCH₃ IA-1230 A¹.2 CH₂COOH CH₂SCH₃ IA-1231 A¹.2 CH₂COOCH₃ CH₂SCH₃ IA-1232 A¹.2 CH₂COOCH₂CH₃ CH₂SCH₃ IA-1233 A¹.2 cyclo-C₃H₅ CH₂SCH₃ IA-1234 A¹.2 cyclo-C₄H₇ CH₂SCH₃ IA-1235 A¹.2 cyclo-C₅H₉ CH₂SCH₃ IA-1236 A¹.2 cyclo-C₆H₁₁ CH₂SCH₃ IA-1237 A¹.2 C₆H₅ CH₂SCH₃ IA-1238 A¹.2 (CH₂)₃SCH₃ (CH₂)₃SCH₃ IA-1239 A¹.2 CH₂S(═O)CH₃ (CH₂)₃SCH₃ IA-1240 A¹.2 CH₂S(═O)₂CH₃ (CH₂)₃SCH₃ IA-1241 A¹.2 CH₂C(═O)CH₃ (CH₂)₃SCH₃ IA-1242 A¹.2 CH₂C(═O)CH₂CH₃ (CH₂)₃SCH₃ IA-1243 A¹.2 CH₂COOH (CH₂)₃SCH₃ IA-1244 A¹.2 CH₂COOCH₃ (CH₂)₃SCH₃ IA-1245 A¹.2 CH₂COOCH₂CH₃ (CH₂)₃SCH₃ IA-1246 A¹.2 cyclo-C₃H₅ (CH₂)₃SCH₃ IA-1247 A¹.2 cyclo-C₄H₇ (CH₂)₃SCH₃ IA-1248 A¹.2 cyclo-C₅H₉ (CH₂)₃SCH₃ IA-1249 A¹.2 cyclo-C₆H₁₁ (CH₂)₃SCH₃ IA-1250 A¹.2 C₆H₅ (CH₂)₃SCH₃ IA-1251 A¹.2 CH₂S(═O)CH₃ CH₂S(═O)CH₃ IA-1252 A¹.2 CH₂S(═O)₂CH₃ CH₂S(═O)CH₃ IA-1253 A¹.2 CH₂C(═O)CH₃ CH₂S(═O)CH₃ IA-1254 A¹.2 CH₂C(═O)CH₂CH₃ CH₂S(═O)CH₃ IA-1255 A¹.2 CH₂COOH CH₂S(═O)CH₃ IA-1256 A¹.2 CH₂COOCH₃ CH₂S(═O)CH₃ IA-1257 A¹.2 CH₂COOCH₂CH₃ CH₂S(═O)CH₃ IA-1258 A¹.2 cyclo-C₃H₅ CH₂S(═O)CH₃ IA-1259 A¹.2 cyclo-C₄H₇ CH₂S(═O)CH₃ IA-1260 A¹.2 cyclo-C₅H₉ CH₂S(═O)CH₃ IA-1261 A¹.2 cyclo-C₆H₁₁ CH₂S(═O)CH₃ IA-1262 A¹.2 C₆H₅ CH₂S(═O)CH₃ IA-1263 A¹.2 CH₂S(═O)₂CH₃ CH₂S(═O)₂CH₃ IA-1264 A¹.2 CH₂C(═O)CH₃ CH₂S(═O)₂CH₃ IA-1265 A¹.2 CH₂C(═O)CH₂CH₃ CH₂S(═O)₂CH₃ IA-1266 A¹.2 CH₂COOH CH₂S(═O)₂CH₃ IA-1267 A¹.2 CH₂COOCH₃ CH₂S(═O)₂CH₃ IA-1268 A¹.2 CH₂COOCH₂CH₃ CH₂S(═O)₂CH₃ IA-1269 A¹.2 cyclo-C₃H₅ CH₂S(═O)₂CH₃ IA-1270 A¹.2 cyclo-C₄H₇ CH₂S(═O)₂CH₃ IA-1271 A¹.2 cyclo-C₅H₉ CH₂S(═O)₂CH₃ IA-1272 A¹.2 cyclo-C₆H₁₁ CH₂S(═O)₂CH₃ IA-1273 A¹.2 C₆H₅ CH₂S(═O)₂CH₃ IA-1274 A¹.2 CH₂C(═O)CH₃ CH₂C(═O)CH₃ IA-1275 A¹.2 CH₂C(═O)CH₂CH₃ CH₂C(═O)CH₃ IA-1276 A¹.2 CH₂COOH CH₂C(═O)CH₃ IA-1277 A¹.2 CH₂COOCH₃ CH₂C(═O)CH₃ IA-1278 A¹.2 CH₂COOCH₂CH₃ CH₂C(═O)CH₃ IA-1279 A¹.2 cyclo-C₃H₅ CH₂C(═O)CH₃ IA-1280 A¹.2 cyclo-C₄H₇ CH₂C(═O)CH₃ IA-1281 A¹.2 cyclo-C₅H₉ CH₂C(═O)CH₃ IA-1282 A¹.2 cyclo-C₆H₁₁ CH₂C(═O)CH₃ IA-1283 A¹.2 C₆H₅ CH₂C(═O)CH₃ IA-1284 A¹.2 CH₂C(═O)CH₂CH₃ CH₂C(═O)CH₂CH₃ IA-1285 A¹.2 CH₂COOH CH₂C(═O)CH₂CH₃ IA-1286 A¹.2 CH₂COOCH₃ CH₂C(═O)CH₂CH₃ IA-1287 A¹.2 CH₂COOCH₂CH₃ CH₂C(═O)CH₂CH₃ IA-1288 A¹.2 cyclo-C₃H₅ CH₂C(═O)CH₂CH₃ IA-1289 A¹.2 cyclo-C₄H₇ CH₂C(═O)CH₂CH₃ IA-1290 A¹.2 cyclo-C₅H₉ CH₂C(═O)CH₂CH₃ IA-1291 A¹.2 cyclo-C₆H₁₁ CH₂C(═O)CH₂CH₃ IA-1292 A¹.2 C₆H₅ CH₂C(═O)CH₂CH₃ IA-1293 A¹.2 CH₂COOH CH₂COOH IA-1294 A¹.2 CH₂COOCH₃ CH₂COOH IA-1295 A¹.2 CH₂COOCH₂CH₃ CH₂COOH IA-1296 A¹.2 cyclo-C₃H₅ CH₂COOH IA-1297 A¹.2 cyclo-C₄H₇ CH₂COOH IA-1298 A¹.2 cyclo-C₅H₉ CH₂COOH IA-1299 A¹.2 cyclo-C₆H₁₁ CH₂COOH IA-1300 A¹.2 C₆H₅ CH₂COOH IA-1301 A¹.2 CH₂COOCH₃ CH₂COOCH₃ IA-1302 A¹.2 CH₂COOCH₂CH₃ CH₂COOCH₃ IA-1303 A¹.2 cyclo-C₃H₅ CH₂COOCH₃ IA-1304 A¹.2 cyclo-C₄H₇ CH₂COOCH₃ IA-1305 A¹.2 cyclo-C₅H₉ CH₂COOCH₃ IA-1306 A¹.2 cyclo-C₆H₁₁ CH₂COOCH₃ IA-1307 A¹.2 C₆H₅ CH₂COOCH₃ IA-1308 A¹.2 CH₂COOCH₂CH₃ CH₂COOCH₂CH₃ IA-1309 A¹.2 cyclo-C₃H₅ CH₂COOCH₂CH₃ IA-1310 A¹.2 cyclo-C₄H₇ CH₂COOCH₂CH₃ IA-1311 A¹.2 cyclo-C₅H₉ CH₂COOCH₂CH₃ IA-1312 A¹.2 cyclo-C₆H₁₁ CH₂COOCH₂CH₃ IA-1313 A¹.2 C₆H₅ CH₂COOCH₂CH₃ IA-1314 A¹.2 cyclo-C₃H₅ cyclo-C₃H₅ IA-1315 A¹.2 cyclo-C₄H₇ cyclo-C₃H₅ IA-1316 A¹.2 cyclo-C₅H₉ cyclo-C₃H₅ IA-1317 A¹.2 cyclo-C₆H₁₁ cyclo-C₃H₅ IA-1318 A¹.2 C₆H₅ cyclo-C₃H₅ IA-1319 A¹.2 cyclo-C₄H₇ cyclo-C₄H₇ IA-1320 A¹.2 cyclo-C₅H₉ cyclo-C₄H₇ IA-1321 A¹.2 cyclo-C₆H₁₁ cyclo-C₄H₇ IA-1322 A¹.2 C₆H₅ cyclo-C₄H₇ IA-1323 A¹.2 cyclo-C₅H₉ cyclo-C₅H₉ IA-1324 A¹.2 cyclo-C₆H₁₁ cyclo-C₅H₉ IA-1325 A¹.2 C₆H₅ cyclo-C₅H₉ IA-1326 A¹.2 cyclo-C₆H₁₁ cyclo-C₆H₁₁ IA-1327 A¹.2 C₆H₅ cyclo-C₆H₁₁ IA-1328 A¹.2 C₆H₅ C₆H₅ Table 883

Compounds of the formula IA (as defined above) wherein Q¹ denotes hydrogen, Q³ denotes CF₃, and A in each case corresponds to a radical of Table D.

Table 884

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes bromine, and A in each case corresponds to a radical of Table D.

Table 885

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes chlorine, and A in each case corresponds to a radical of Table D.

Table 886

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₃, and A in each case corresponds to a radical of Table D.

Table 887

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₃, and A in each case corresponds to a radical of Table D.

Table 888

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCHCH₂, and A in each case corresponds to a radical of Table D.

Table 889

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes ethoxy, and A in each case corresponds to a radical of Table D.

Table 890

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a radical of Table D.

Table 891

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂CH═CH₂, and A in each case corresponds to a radical of Table D.

Table 892

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂CCH, and A in each case corresponds to a radical of Table D.

Table 893

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂OCH₃, and A in each case corresponds to a radical of Table D.

Table 894

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 895

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂SCH₃, and A in each case corresponds to a radical of Table D.

Table 896

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 897

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂S(═O)CH₃, and A in each case corresponds to a radical of Table D.

Table 898

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 899

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a radical of Table D.

Table 900

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 901

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a radical of Table D.

Table 902

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 903

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a radical of Table D.

Table 904

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a radical of Table D.

Table 905

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OC(═O)CF₃, and A in each case corresponds to a radical of Table D.

Table 906

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes NHCH₂CF₃, and A in each case corresponds to a radical of Table D.

Table 907

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a radical of Table D.

Table 908

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a radical of Table D.

Table 909

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a radical of Table D.

Table 910

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a radical of Table D.

Table 911

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a radical of Table D.

Table 912

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂CN, and A in each case corresponds to a radical of Table D.

Table 913

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes OCH₂NO₂, and A in each case corresponds to a radical of Table D.

Table 914

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes cyclopropyloxy, and A in each case corresponds to a radical of Table D.

Table 915

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a radical of Table D.

Table 916

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a radical of Table D.

Table 917

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH═NOCH₃, and A in each case corresponds to a radical of Table D.

Table 918

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH═NOCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 919

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a radical of Table D.

Table 920

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a radical of Table D.

Table 921

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a radical of Table D.

Table 922

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 923

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a radical of Table D.

Table 924

Compounds of the formula IA wherein Q¹ denotes hydrogen, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a radical of Table D.

Table 925

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CF₃, and A in each case corresponds to a radical of Table D.

Table 926

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes bromine, and A in each case corresponds to a radical of Table D.

Table 927

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes chlorine, and A in each case corresponds to a radical of Table D.

Table 928

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₃, and A in each case corresponds to a radical of Table D.

Table 929

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₃, and A in each case corresponds to a radical of Table D.

Table 930

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCHCH₂, and A in each case corresponds to a radical of Table D.

Table 931

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes ethoxy, and A in each case corresponds to a radical of Table D.

Table 932

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a radical of Table D.

Table 933

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂CH═CH₂, and A in each case corresponds to a radical of Table D.

Table 934

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂CCH, and A in each case corresponds to a radical of Table D.

Table 935

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂OCH₃, and A in each case corresponds to a radical of Table D.

Table 936

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 937

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂SCH₃, and A in each case corresponds to a radical of Table D.

Table 938

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 939

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂S(═O)CH₃, and A in each case corresponds to a radical of Table D.

Table 940

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 941

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a radical of Table D.

Table 942

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 943

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a radical of Table D.

Table 944

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 945

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a radical of Table D.

Table 946

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a radical of Table D.

Table 947

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OC(═O)CF₃, and A in each case corresponds to a radical of Table D.

Table 948

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes NHCH₂CF₃, and A in each case corresponds to a radical of Table D.

Table 949

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a radical of Table D.

Table 950

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a radical of Table D.

Table 951

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a radical of Table D.

Table 952

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a radical of Table D.

Table 953

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a radical of Table D.

Table 954

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂CN, and A in each case corresponds to a radical of Table D.

Table 955

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes OCH₂NO₂, and A in each case corresponds to a radical of Table D.

Table 956

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes cyclopropyloxy, and A in each case corresponds to a radical of Table D.

Table 957

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a radical of Table D.

Table 958

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a radical of Table D.

Table 959

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH═NOCH₃, and A in each case corresponds to a radical of Table D.

Table 960

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH═NOCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 961

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a radical of Table D.

Table 962

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a radical of Table D.

Table 963

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a radical of Table D.

Table 964

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 965

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a radical of Table D.

Table 966

Compounds of the formula IA wherein Q¹ denotes chlorine, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a radical of Table D.

Table 967

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CF₃, and A in each case corresponds to a radical of Table D.

Table 968

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes bromine, and A in each case corresponds to a radical of Table D.

Table 969

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes chlorine, and A in each case corresponds to a radical of Table D.

Table 970

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₃, and A in each case corresponds to a radical of Table D.

Table 971

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₃, and A in each case corresponds to a radical of Table D.

Table 972

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCHCH₂, and A in each case corresponds to a radical of Table D.

Table 973

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes ethoxy, and A in each case corresponds to a radical of Table D.

Table 974

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a radical of Table D.

Table 975

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂CH═CH₂, and A in each case corresponds to a radical of Table D.

Table 976

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂CCH, and A in each case corresponds to a radical of Table D.

Table 977

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂OCH₃, and A in each case corresponds to a radical of Table D.

Table 978

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 979

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂SCH₃, and A in each case corresponds to a radical of Table D.

Table 980

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 981

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂S(═O)CH₃, and A in each case corresponds to a radical of Table D.

Table 982

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 983

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a radical of Table D.

Table 984

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 985

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a radical of Table D.

Table 986

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 987

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a radical of Table D.

Table 988

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a radical of Table D.

Table 989

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OC(═O)CF₃, and A in each case corresponds to a radical of Table D.

Table 990

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes NHCH₂CF₃, and A in each case corresponds to a radical of Table D.

Table 991

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a radical of Table D.

Table 992

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a radical of Table D.

Table 993

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a radical of Table D.

Table 994

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a radical of Table D.

Table 995

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a radical of Table D.

Table 996

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂CN, and A in each case corresponds to a radical of Table D.

Table 997

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes OCH₂NO₂, and A in each case corresponds to a radical of Table D.

Table 998

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes cyclopropyloxy, and A in each case corresponds to a radical of Table D.

Table 999

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a radical of Table D.

Table 1000

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a radical of Table D.

Table 1001

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH═NOCH₃, and A in each case corresponds to a radical of Table D.

Table 1002

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH═NOCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1003

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a radical of Table D.

Table 1004

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a radical of Table D.

Table 1005

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a radical of Table D.

Table 1006

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1007

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a radical of Table D.

Table 1008

Compounds of the formula IA wherein Q¹ denotes bromine, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a radical of Table D.

Table 1009

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CF₃, and A in each case corresponds to a radical of Table D.

Table 1010

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes bromine, and A in each case corresponds to a radical of Table D.

Table 1011

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes chlorine, and A in each case corresponds to a radical of Table D.

Table 1012

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₃, and A in each case corresponds to a radical of Table D.

Table 1013

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₃, and A in each case corresponds to a radical of Table D.

Table 1014

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCHCH₂, and A in each case corresponds to a radical of Table D.

Table 1015

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes ethoxy, and A in each case corresponds to a radical of Table D.

Table 1016

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a radical of Table D.

Table 1017

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂CH═CH₂, and A in each case corresponds to a radical of Table D.

Table 1018

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂CCH, and A in each case corresponds to a radical of Table D.

Table 1019

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂OCH₃, and A in each case corresponds to a radical of Table D.

Table 1020

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1021

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂SCH₃, and A in each case corresponds to a radical of Table D.

Table 1022

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1023

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂S(═O)CH₃, and A in each case corresponds to a radical of Table D.

Table 1024

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1025

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1026

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1027

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1028

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1029

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a radical of Table D.

Table 1030

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a radical of Table D.

Table 1031

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OC(═O)CF₃, and A in each case corresponds to a radical of Table D.

Table 1032

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes NHCH₂CF₃, and A in each case corresponds to a radical of Table D.

Table 1033

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a radical of Table D.

Table 1034

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a radical of Table D.

Table 1035

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a radical of Table D.

Table 1036

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a radical of Table D.

Table 1037

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a radical of Table D.

Table 1038

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂CN, and A in each case corresponds to a radical of Table D.

Table 1039

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes OCH₂NO₂, and A in each case corresponds to a radical of Table D.

Table 1040

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes cyclopropyloxy, and A in each case corresponds to a radical of Table D.

Table 1041

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a radical of Table D.

Table 1042

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a radical of Table D.

Table 1043

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH═NOCH₃, and A in each case corresponds to a radical of Table D.

Table 1044

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH═NOCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1045

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a radical of Table D.

Table 1046

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a radical of Table D.

Table 1047

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a radical of Table D.

Table 1048

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1049

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a radical of Table D.

Table 1050

Compounds of the formula IA wherein Q¹ denotes fluorine, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a radical of Table D.

Table 1051

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CF₃, and A in each case corresponds to a radical of Table D.

Table 1052

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes bromine, and A in each case corresponds to a radical of Table D.

Table 1053

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes chlorine, and A in each case corresponds to a radical of Table D.

Table 1054

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₃, and A in each case corresponds to a radical of Table D.

Table 1055

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₃, and A in each case corresponds to a radical of Table D.

Table 1056

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCHCH₂, and A in each case corresponds to a radical of Table D.

Table 1057

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes ethoxy, and A in each case corresponds to a radical of Table D.

Table 1058

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a radical of Table D.

Table 1059

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂CH═CH₂, and A in each case corresponds to a radical of Table D.

Table 1060

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂CCH, and A in each case corresponds to a radical of Table D.

Table 1061

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂OCH₃, and A in each case corresponds to a radical of Table D.

Table 1062

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1063

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂SCH₃, and A in each case corresponds to a radical of Table D.

Table 1064

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1065

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂S(═O)CH₃, and A in each case corresponds to a radical of Table D.

Table 1066

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1067

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1068

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1069

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1070

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1071

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a radical of Table D.

Table 1072

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a radical of Table D.

Table 1073

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OC(═O)CF₃, and A in each case corresponds to a radical of Table D.

Table 1074

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes NHCH₂CF₃, and A in each case corresponds to a radical of Table D.

Table 1075

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a radical of Table D.

Table 1076

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a radical of Table D.

Table 1077

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a radical of Table D.

Table 1078

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a radical of Table D.

Table 1079

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a radical of Table D.

Table 1080

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂CN, and A in each case corresponds to a radical of Table D.

Table 1081

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes OCH₂NO₂, and A in each case corresponds to a radical of Table D.

Table 1082

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes cyclopropyloxy, and A in each case corresponds to a radical of Table D.

Table 1083

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a radical of Table D.

Table 1084

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a radical of Table D.

Table 1085

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH═NOCH₃, and A in each case corresponds to a radical of Table D.

Table 1086

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH═NOCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1087

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a radical of Table D.

Table 1088

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a radical of Table D.

Table 1089

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a radical of Table D.

Table 1090

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1091

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a radical of Table D.

Table 1092

Compounds of the formula IA wherein Q¹ denotes iodine, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a radical of Table D.

Table 1093

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CF₃, and A in each case corresponds to a radical of Table D.

Table 1094

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes bromine, and A in each case corresponds to a radical of Table D.

Table 1095

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes chlorine, and A in each case corresponds to a radical of Table D.

Table 1096

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₃, and A in each case corresponds to a radical of Table D.

Table 1097

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₃, and A in each case corresponds to a radical of Table D.

Table 1098

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCHCH₂, and A in each case corresponds to a radical of Table D.

Table 1099

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes ethoxy, and A in each case corresponds to a radical of Table D.

Table 1100

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a radical of Table D.

Table 1101

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂CH═CH₂, and A in each case corresponds to a radical of Table D.

Table 1102

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂CCH, and A in each case corresponds to a radical of Table D.

Table 1103

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂OCH₃, and A in each case corresponds to a radical of Table D.

Table 1104

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1105

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂SCH₃, and A in each case corresponds to a radical of Table D.

Table 1106

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1107

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂S(═O)CH₃, and A in each case corresponds to a radical of Table D.

Table 1108

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1109

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1110

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1111

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1112

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1113

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a radical of Table D.

Table 1114

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a radical of Table D.

Table 1115

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OC(═O)CF₃, and A in each case corresponds to a radical of Table D.

Table 1116

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes NHCH₂CF₃, and A in each case corresponds to a radical of Table D.

Table 1117

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a radical of Table D.

Table 1118

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a radical of Table D.

Table 1119

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a radical of Table D.

Table 1120

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a radical of Table D.

Table 1121

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a radical of Table D.

Table 1122

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂CN, and A in each case corresponds to a radical of Table D.

Table 1123

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes OCH₂NO₂, and A in each case corresponds to a radical of Table D.

Table 1124

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes cyclopropyloxy, and A in each case corresponds to a radical of Table D.

Table 1125

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a radical of Table D.

Table 1126

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a radical of Table D.

Table 1127

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH═NOCH₃, and A in each case corresponds to a radical of Table D.

Table 1128

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH═NOCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1129

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a radical of Table D.

Table 1130

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a radical of Table D.

Table 1131

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a radical of Table D.

Table 1132

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1133

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a radical of Table D.

Table 1134

Compounds of the formula IA wherein Q¹ denotes cyano, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a radical of Table D.

Table 1135

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CF₃, and A in each case corresponds to a radical of Table D.

Table 1136

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes bromine, and A in each case corresponds to a radical of Table D.

Table 1137

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes chlorine, and A in each case corresponds to a radical of Table D.

Table 1138

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₃, and A in each case corresponds to a radical of Table D.

Table 1139

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₃, and A in each case corresponds to a radical of Table D.

Table 1140

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCHCH₂, and A in each case corresponds to a radical of Table D.

Table 1141

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes ethoxy, and A in each case corresponds to a radical of Table D.

Table 1142

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂CHFOCH₃, and A in each case corresponds to a radical of Table D.

Table 1143

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂CH═CH₂, and A in each case corresponds to a radical of Table D.

Table 1144

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂CCH, and A in each case corresponds to a radical of Table D.

Table 1145

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂OCH₃, and A in each case corresponds to a radical of Table D.

Table 1146

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂OCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1147

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂SCH₃, and A in each case corresponds to a radical of Table D.

Table 1148

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂SCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1149

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂S(═O)CH₃, and A in each case corresponds to a radical of Table D.

Table 1150

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂S(═O)CH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1151

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂S(═O)₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1152

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂S(═O)₂CH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1153

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes —OS(═O)₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1154

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes —OS(═O)₂CH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1155

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes —OS(═O)₂CH₂CF₃, and A in each case corresponds to a radical of Table D.

Table 1156

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes —OS(═O)₂CClF₂, and A in each case corresponds to a radical of Table D.

Table 1157

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OC(═O)CF₃, and A in each case corresponds to a radical of Table D.

Table 1158

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes NHCH₂CF₃, and A in each case corresponds to a radical of Table D.

Table 1159

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂-cyclopropyl, and A in each case corresponds to a radical of Table D.

Table 1160

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂C(Cl)═CH₂, and A in each case corresponds to a radical of Table D.

Table 1161

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂CH═CF₂, and A in each case corresponds to a radical of Table D.

Table 1162

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes NHS(═O)₂CF₃, and A in each case corresponds to a radical of Table D.

Table 1163

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes NHC(═O)CF₃, and A in each case corresponds to a radical of Table D.

Table 1164

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂CN, and A in each case corresponds to a radical of Table D.

Table 1165

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes OCH₂NO₂, and A in each case corresponds to a radical of Table D.

Table 1166

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes cyclopropyloxy, and A in each case corresponds to a radical of Table D.

Table 1167

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂OCHF₂, and A in each case corresponds to a radical of Table D.

Table 1168

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH₂S(═O)₂CHF₂, and A in each case corresponds to a radical of Table D.

Table 1169

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH═NOCH₃, and A in each case corresponds to a radical of Table D.

Table 1170

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH═NOCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1171

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH═NOCH(CH₃)₂ and A in each case corresponds to a radical of Table D.

Table 1172

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes CH═NOC(CH₃)₃, and A in each case corresponds to a radical of Table D.

Table 1173

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes C(CH₃)═NOCH₃, and A in each case corresponds to a radical of Table D.

Table 1174

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes C(CH₃)═NOCH₂CH₃, and A in each case corresponds to a radical of Table D.

Table 1175

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes C(CH₃)═NOCH(CH₃)₂, and A in each case corresponds to a radical of Table D.

Table 1176

Compounds of the formula IA wherein Q¹ denotes methyl, Q³ denotes C(CH₃)═NOC(CH₃)₃, and A in each case corresponds to a radical of Table D.

TABLE D selected radicals A A.11

A.12

A.13

A.14

A.15

A.14

A.15

A.16

A.11

A.12

A.13

A.14

A.15

A.11

A.12

A.13

A.14

A.15

A.11

A.12

A.13

A.14

A.15

A.15

A.12

A.13

A.14

A.11

A.12

A.13

The compounds of the formula I are especially suitable for efficiently combating the following pests:

insects from the order of the lepidopterans (Lepidoptera), for example Agrotis ypsilon, Agrotis segetum, Alabama argillacea, Anticarsia gemmatalis, Argyresthia conjugella, Autographa gamma, Bupalus piniarius, Cacoecia murinana, Capua reticulana, Cheimatobia brumata, Choristoneura fumiferana, Choristoneura occidentalis, Cirphis unipuncta, Cydia pomonella, Dendrolimus pini, Diaphania nitidalis, Diatraea grandiosella, Earias insulana, Elasmopalpus lignosellus, Eupoecilia ambiguella, Evetria bouliana, Feltia subterranea, Galleria mellonella, Grapholitha funebrana, Grapholitha molesta, Heliothis armigera, Heliothis virescens, Heliothis zea, Hellula undalis, Hibernia defoliaria, Hyphantria cunea, Hyponomeuta malinellus, Keiferia lycopersicella, Lambdina fiscellaria, Laphygma exigua, Leucoptera coffeella, Leucoptera scitella, Lithocolletis blancardella, Lobesia botrana, Loxostege sticticalis, Lymantria dispar, Lymantria monacha, Lyonetia clerkella, Malacosoma neustria, Mamestra brassicae, Orgyia pseudotsugata, Ostrinia nubilalis, Panolis flammea, Pectinophora gossypiella, Peridroma saucia, Phalera bucephala, Phthorimaea operculella, Phyllocnistis citrella, Pieris brassicae, Plathypena scabra, Plutella xylostella, Pseudoplusia includens, Rhyacionia frustrana, Scrobipalpula absoluta, Sitotroga cerealella, Sparganothis pilleriana, Spodoptera frugiperda, Spodoptera littoralis, Spodoptera litura, Thaumatopoea pityocampa, Tortrix viridana, Trichoplusia ni and Zeiraphera canadensis, beetles (Coleoptera), for example Agrilus sinuatus, Agriotes lineatus, Agriotes obscurus, Amphimallus solstitialis, Anisandrus dispar, Anthonomus grandis, Anthonomus pomorum, Aphthona euphoridae, Athous haemorrhoidalis, Atomaria linearis, Blastophagus piniperda, Blitophaga undata, Bruchus rufimanus, Bruchus pisorum, Bruchus lentis, Byctiscus betulae, Cassida nebulosa, Cerotoma trifurcata, Cetonia aurata, Ceuthorrhynchus assimilis, Ceuthorrhynchus napi, Chaetocnema tibialis, Conoderus vespertinus, Crioceris asparagi, Ctenicera ssp., Diabrotica longicornis, Diabrotica semipunctata, Diabrotica 12-punctata Diabrotica speciosa, Diabrotica virgifera, Epilachna varivestis, Epitrix hirtipennis, Eutinobothrus braslliensis, Hylobius abietis, Hypera brunneipennis, Hypera postica, Ips typographus, Lema bilineata, Lema melanopus, Leptinotarsa decemlineata, Limonius californicus, Lissorhoptrus oryzophilus, Melanotus communis, Meligethes aeneus, Melolontha hippocastani, Melolontha melolontha, Oulema oryzae, Ortiorrhynchus sulcatus, Otiorrhynchus ovatus, Phaedon cochleariae, Phyllobius pyri, Phyllotreta chrysocephala, Phyllophaga sp., Phyllopertha horticola, Phyllotreta nemorum, Phyllotreta striolata, Popillia japonica, Sitona lineatus and Sitophilus granaria, flies, mosquitoes (Diptera), e.g. Aedes aegypti, Aedes albopictus, Aedes vexans, Anastrepha ludens, Anopheles maculipennis, Anopheles crucians, Anopheles albimanus, Anopheles gambiae, Anopheles freeborni, Anopheles leucosphyrus, Anopheles minimus, Anopheles quadrimaculatus, Calliphora vicina, Ceratitis capitata, Chrysomya bezziana, Chrysomya hominivorax, Chrysomya macellaria, Chrysops discalis, Chrysops silacea, Chrysops atlanticus, Cochliomyia hominivorax, Contarinia sorghicola Cordylobia anthropophaga, Culicoides furens, Culex pipiens, Culex nigripalpus, Culex quinquefasciatus, Culex tarsalis, Culiseta inornata, Culiseta melanura, Dacus cucurbitae, Dacus oleae, Dasineura brassicae, Delia antique, Delia coarctata, Delia platura, Delia radicum, Dermatobia hominis, Fannia canicularis, Geomyza Tripunctata, Gasterophilus intestinalis, Glossina morsitans, Glossina palpalis, Glossina fuscipes, Glossina tachinoides, Haematobia irritans, Haplodiplosis equestris, Hippelates spp., Hylemyia platura, Hypoderma lineata, Leptoconops torrens, Liriomyza sativae, Liriomyza trifolii, Lucilia caprina, Lucilia cuprina, Lucilia sericata, Lycoria pectoralis, Mansonia titillanus, Mayetiola destructor, Musca domestics, Muscina stabulans, Oestrus ovis, Opomyza florum, Oscinella frit, Pegomya hysocyami, Phorbia antiqua, Phorbia brassicae, Phorbia coarctata, Phlebotomus argentipes, Psorophora columbiae, Psila rosae, Psorophora discolor, Prosimulium mixtum, Rhagoletis cerasi, Rhagoletis pomonella, Sarcophaga haemorrhoidalis, Sarcophaga sp., Simulium vittatum, Stomoxys calcitrans, Tabanus bovinus, Tabanus atratus, Tabanus lineola, and Tabanus similis, Tipula oleracea, and Tipula paludosa thrips (Thysanoptera), e.g. Dichromothrips corbetti, Dichromothrips ssp, Frankliniella fusca, Frankliniella occidentalis, Frankliniella tritici, Scirtothrips citri, Thrips oryzae, Thrips palmi and Thrips tabaci, termites (Isoptera), e.g. Calotermes flavicollis, Leucotermes flavipes, Heterotermes aureus, Reticulitermes flavipes, Reticulitermes virginicus, Reticulitermes lucifugus, Termes natalensis, and Coptotermes formosanus, cockroaches (Blattaria—Blattodea), e.g. Blattella germanica, Blattella asahinae, Periplaneta americana, Periplaneta japonica, Periplaneta brunnea, Periplaneta fuligginosa, Periplaneta australasiae, and Blatta orientalis, true bugs (Hemiptera), e.g. Acrosternum hiare, Blissus leucopterus, Cyrtopeltis notatus, Dysdercus cingulatus, Dysdercus intermedius, Eurygaster integriceps, Euschistus impictiventris, Leptoglossus phyllopus, Lygus lineolaris, Lygus pratensis, Nezara viridula, Piesma quadrata, Solubea insularis, Thyanta perditor, Acyrthosiphon onobrychis, Adelges laricis, Aphidula nasturtii, Aphis fabae, Aphis forbesi, Aphis pomi, Aphis gossypii, Aphis grossulariae, Aphis schneideri, Aphis spiraecola, Aphis sambuci, Acyrthosiphon pisum, Aulacorthum solani, Bemisia argentifolii, Brachycaudus cardui, Brachycaudus helichrysi, Brachycaudus persicae, Brachycaudus prunicola, Brevicoryne brassicae, Capitophorus horni, Cerosipha gossypii, Chaetosiphon fragaefolii, Cryptomyzus ribis, Dreyfusia nordmannianae, Dreyfusia piceae, Dysaphis radicola, Dysaulacorthum pseudosolani, Dysaphis plantaginea, Dysaphis pyri, Empoasca fabae, Hyalopterus pruni, Hyperomyzus lactucae, Macrosiphum avenae, Macrosiphum euphorbiae, Macrosiphon rosae, Megoura viciae, Melanaphis pyrarius, Metopolophium dirhodum, Myzus persicae, Myzus ascalonicus, Myzus cerasi, Myzus varians, Nasonovia ribis-nigri, Nilaparvata lugens, Pemphigus bursarius, Perkinsiella saccharicida, Phorodon humuli, Psylla mali, Psylla piri, Rhopalomyzus ascalonicus, Rhopalosiphum maidis, Rhopalosiphum padi, Rhopalosiphum insertum, Sappaphis mala, Sappaphis mali, Schizaphis graminum, Schilzoneura lanuginosa, Sitobion avenae, Trialeurodes vaporariorum, Toxoptera aurantiiand, Viteus vitifolii, Cimex lectularius, Cimex hemipterus, Reduvius senilis, Triatoma spp., and Arilus critatus. ants, bees, wasps, sawflies (Hymenoptera), e.g. Athalia rosae, Atta cephalotes, Atta capiguara, Atta cephalotes, Atta laevigata, Atta robusta, Atta sexdens, Atta texana, Crematogaster spp., Hoplocampa minuta, Hoplocampa testudinea, Monomorium pharaonis, Solenopsis geminata, Solenopsis invicta, Solenopsis richteri, Solenopsis xyloni, Pogonomyrmex barbatus, Pogonomyrmex californicus, Pheidole megacephala, Dasymutilla occidentalis, Bombus spp. Vespula squamosa, Paravespula vulgaris, Paravespula pennsylvanica, Paravespula germanica, Dolichovespula maculata, Vespa crabro, Polistes rubiginosa, Camponotus floridanus, and Linepithema humile, crickets, grasshoppers, locusts (Orthoptera), e.g. Acheta domestica, Gryllotalpa gryllotalpa, Locusta migratoria, Melanoplus bivittatus, Melanoplus femurrubrum, Melanoplus mexicanus, Melanoplus sanguinipes, Melanoplus spretus, Nomadacris septemfasciata, Schistocerca americana, Schistocerca gregaria, Dociostaurus maroccanus, Tachycines asynamorus, Oedaleus senegalensis, Zonozerus variegatus, Hieroglyphus daganensis, Kraussaria angulifera, Calliptamus italicus, Chortoicetes terminifera, and Locustana pardalina, Arachnoidea, such as arachnids (Acarina), e.g. of the families Argasidae, Ixodidae and Sarcoptidae, such as Amblyomma americanum, Amblyomma variegatum, Amblyomma maculatum, Argas persicus, Boophilus annulatus, Boophilus decoloratus, Boophilus microplus, Dermacentor silvarum, Dermacentor andersoni, Dermacentor variablis, Hyalomma truncatum, Ixodes ricinus, Ixodes rubicundus, Ixodes scapularis, Ixodes holocyclus, Ixodes pacificus, Ornithodorus moubata, Ornithodorus hermsi, Ornithodorus turicata, Ornithonyssus bacoti, Otobius megnini, Dermanyssus gallinae, Psoroptes ovis, Rhipicephalus sanguineus, Rhipicephalus appendiculatus, Rhipicephalus evertsi, Sarcoptes scabiei, and Eriophyidae spp. such as Aculus schlechtendali, Phyllocoptrata oleivora and Eriophyes sheldoni; Tarsonemidae spp. such as Phytonemus pallidus and Polyphagotarsonemus latus; Tenuipalpidae spp. such as Brevipalpus phoenicis; Tetranychidae spp. such as Tetranychus cinnabarinus, Tetranychus kanzawai, Tetranychus pacificus, Tetranychus telarius and Tetranychus urticae, Panonychus ulmi, Panonychus citri, and Oligonychus pratensis; Araneida, e.g. Latrodectus mactans, and Loxosceles reclusa, fleas (Siphonaptera), e.g. Ctenocephalides felis, Ctenocephafides canis, Xenopsylla cheopis, Pulex irritans, Tunga penetrans, and Nosopsyllus fasciatus, silverfish, firebrat (Thysanura), e.g. Lepisma saccharina and Thermobia domestica, centipedes (Chilopoda), e.g. Scutigera coleoptrata, millipedes (Diplopoda), e.g. Narceus spp., Earwigs (Dermaptera), e.g. forficula auricularia, lice (Phthiraptera), e.g. Pediculus humanus capitis, Pediculus humanus corporis, Pthirus pubis, Haematopinus eurysternus, Haematopinus suis, Linognathus vituli, Bovicola bovis, Menopon gallinae, Menacanthus stramineus and Solenopotes capillatus, Plant parasitic nematodes such as root-knot nematodes, Meloidogyne arenaria, Meloidogyne chitwoodi, Meloidogyne exigua, Meloidogyne hapla, Meloidogyne incognita, Meloidogyne javanica and other Meloidogyne species; cyst nematodes, Globodera rostochiensis, Globodera pallida, Globodera tabacum and other Globodera species, Heterodera avenae, Heterodera glycines, Heterodera schachtii, Heterodera trifolii and other Heterodera species; seed gall nematodes, Anguina funesta, Anguina tritici and other Anguina species; stem and foliar nematodes, Aphelenchoides besseyi, Aphelenchoides fragariae, Aphelenchoides ritzemabosi and other Aphelenchoides species; sting nematodes, Belonolaimus longicaudatus and other Belonolaimus species; pine nematodes, Bursaphelenchus xylophilus and other Bursaphelenchus species; ring nematodes, Criconema species, Criconemella species, Criconemodes species, and Mesocriconema species; stem and bulb nematodes, Ditylenchus destructor, Ditylenchus dipsaci, Ditylenchus myceliophagus and other Ditylenchus species; awl nematodes, Dolichodorus species; spiral nematodes, Helicotylenchus dihystera, Helicotylenchus multicinctus and other Helicotylenchus species, Rotylenchus robustus and other Rotylenchus species; sheath nematodes, Hemicycliophora species and Hemicriconemoides species; Hirshmanniella species; lance nematodes, Hoplolaimus columbus, Hoplolaimus galeatus and other Hoplolaimus species, false root-knot nematodes, Nacobbus aberrans and other Nacobbus species; needle nematodes, Longidorus elongates and other Longidorus species; pin nematodes, Paratylenchus species; lesion nematodes, Pratylenchus brachyurus, Pratylenchus coffeae, Pratylenchus curvitatus, Pratylenchus goodeyi, Pratylencus neglectus, Pratylenchus penetrans, Pratylenchus scribneri, Pratylenchus vulnus, Pratylenchus zeae and other Pratylenchus species; Radinaphelenchus cocophilus and other Radinaphelenchus species; burrowing nematodes, Radopholus formis and other Radopholus species; reniform nematodes, Rotylenchulus reniformis and other Rotylenchulus species; Scutellonema species; stubby root nematodes, Trichodorus primitivus and other Trichodorus species; Paratrichodorus minor and other Paratrichodorus species, stunt nematodes, Tylenchorhynchus claytoni, Tylenchorhynchus dubius and other Tylenchorhynchus species and Merlinius species; citrus nematodes, Tylenchulus semipenetrans and other Tylenchulus species; dagger nematodes, Xiphinema americanum, Xiphinema index, Xiphinema diversicaudatum and other Xiphinema species, and other plant parasitic nematode species.

The formulations are prepared in a known manner (see e.g. for review U.S. Pat. No. 3,060,084, EP-A 707 445 (for liquid concentrates), Browning, “Agglomeration”, Chemical Engineering, Dec. 4, 1967, 147-48, Perry's Chemical Engineer's Handbook, 4th Ed., McGraw-Hill, New York, 1963, pages 8-57 and et seq. WO 91/13546, U.S. Pat. No. 4,172,714, U.S. Pat. No. 4,144,050, U.S. Pat. No. 3,920,442, U.S. Pat. No. 5,180,587, U.S. Pat. No. 5,232,701, U.S. Pat. No. 5,208,030, GB 2,095,558, U.S. Pat. No. 3,299,566, Klingman, Weed Control as a Science, John Wiley and Sons, Inc., New York, 1961, Hance et al., Weed Control Handbook, 8th Ed., Blackwell Scientific Publications, Oxford, 1989 and Mollet, H., Grubemann, A., Formulation technology, Wiley VCH Verlag GmbH, Weinheim (Germany), 2001, 2. D. A. Knowles, Chemistry and Technology of Agrochemical Formulations, Kluwer Academic Publishers, Dordrecht, 1998 (ISBN 0-7514-0443-8), for example by extending the active compound with auxiliaries suitable for the formulation of agrochemicals, such as solvents and/or carriers, if desired emulsifiers, surfactants and dispersants, preservatives, anti-foaming agents, anti-freezing agents, for seed treatment formulation also optionally colorants and binders.

Examples of suitable solvents are water, aromatic solvents (for example Solvesso products, xylene), paraffins (for example mineral oil fractions), alcohols (for example methanol, butanol, pentanol, benzyl alcohol), ketones (for example cyclohexanone, gamma-butyrolactone), pyrrolidones (NMP, NOP), acetates (glycol diacetate), glycols, fatty acid dimethylamides, fatty acids and fatty acid esters. In principle, solvent mixtures may also be used.

Examples of suitable carriers are ground natural minerals (for example kaolins, clays, talc, chalk) and ground synthetic minerals (for example highly disperse silica, silicates).

Suitable emulsifiers are nonionic and anionic emulsifiers (for example polyoxyethylene fatty alcohol ethers, alkylsulfonates and arylsulfonates).

Examples of dispersants are lignin-sulfite waste liquors and methylcellulose.

Suitable surfactants used are alkali metal, alkaline earth metal and ammonium salts of lignosulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid, dibutylnaphthalenesulfonic acid, alkylarylsulfonates, alkyl sulfates, alkylsulfonates, fatty alcohol sulfates, fatty acids and sulfated fatty alcohol glycol ethers, furthermore condensates of sulfonated naphthalene and naphthalene derivatives with formaldehyde, condensates of naphthalene or of naphthalenesulfonic acid with phenol and formaldehyde, polyoxyethylene octylphenol ether, ethoxylated isooctylphenol, octylphenol, nonylphenol, alkylphenol polyglycol ethers, tributylphenyl polyglycol ether, tristearylphenyl polyglycol ether, alkylaryl polyether alcohols, alcohol and fatty alcohol ethylene oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl ethers, ethoxylated polyoxypropylene, lauryl alcohol polyglycol ether acetal, sorbitol esters, lignosulfite waste liquors and methylcellulose.

Substances which are suitable for the preparation of directly sprayable solutions, emulsions, pastes or oil dispersions are mineral oil fractions of medium to high boiling point, such as kerosene or diesel oil, furthermore coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, for example toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes or their derivatives, methanol, ethanol, propanol, butanol, cyclohexanol, cyclohexanone, isophorone, highly polar solvents, for example dimethyl sulfoxide, N-methylpyrrolidone or water.

Also anti-freezing agents such as glycerin, ethylene glycol, propylene glycol and bactericides such as can be added to the formulation.

Suitable antifoaming agents are for example antifoaming agents based on silicon or magnesium stearate.

Powders, materials for spreading and dustable products can be prepared by mixing or concomitantly grinding the active substances with a solid carrier.

Granules, for example coated granules, impregnated granules and homogeneous granules, can be prepared by binding the active compounds to solid carriers. Examples of solid carriers are mineral earths such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers, such as, for example, ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas, and products of vegetable origin, such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powders and other solid carriers.

In general, the formulations comprise from 0.01 to 95% by weight, preferably from 0.1 to 90% by weight, of the active compound(s). In this case, the active compound(s) are employed in a purity of from 90% to 100% by weight, preferably 95% to 100% by weight (according to NMR spectrum).

The compounds of formula I can be used as such, in the form of their formulations or the use forms prepared therefrom, for example in the form of directly sprayable solutions, powders, suspensions or dispersions, emulsions, oil dispersions, pastes, dustable products, materials for spreading, or granules, by means of spraying, atomizing, dusting, spreading or pouring. The use forms depend entirely on the intended purposes; they are intended to ensure in each case the finest possible distribution of the active compound(s) according to the invention.

Aqueous use forms can be prepared from emulsion concentrates, pastes or wettable powders (sprayable powders, oil dispersions) by adding water. To prepare emulsions, pastes or oil dispersions, the substances, as such or dissolved in an oil or solvent, can be homogenized in water by means of a wetter, tackifier, dispersant or emulsifier. However, it is also possible to prepare concentrates composed of active substance, wetter, tackifier, dispersant or emulsifier and, if appropriate, solvent or oil, and such concentrates are suitable for dilution with water.

The active compound concentrations in the ready-to-use preparations can be varied within relatively wide ranges. In general, they are from 0.0001 to 10%, preferably from 0.01 to 1% per weight.

The active compound(s) may also be used successfully in the ultra-low-volume process (ULV), it being possible to apply formulations comprising over 95% by weight of active compound, or even to apply the active compound without additives.

The following are examples of formulations: 1. Products for dilution with water for foliar applications. For seed treatment purposes, such products may be applied to the seed diluted or undiluted.

A) Water-Soluble Concentrates (SL, LS)

10 parts by weight of the active compound(s) are dissolved in 90 parts by weight of water or a water-soluble solvent. As an alternative, welters or other auxiliaries are added. The active compound(s) dissolves upon dilution with water, whereby a formulation with 10% (w/w) of active compound(s) is obtained.

B) Dispersible Concentrates (DC)

20 parts by weight of the active compound(s) are dissolved in 75 parts by weight of cyclohexanone with addition of 10 parts by weight of a dispersant, for example polyvinylpyrrolidone. Dilution with water gives a dispersion, whereby a formulation with 20% (w/w) of active compound(s) is obtained.

C) Emulsifiable Concentrates (EC)

15 parts by weight of the active compound(s) are dissolved in 75 parts by weight of xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight). Dilution with water gives an emulsion, whereby a formulation with 15% (w/w) of active compound(s) is obtained.

D) Emulsions (EW, EO, ES)

40 parts by weight of the active compound(s) are dissolved in 35 parts by weight of xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight). This mixture is introduced into 30 parts by weight of water by means of an emulsifier machine (e.g. Ultraturrax) and made into a homogeneous emulsion. Dilution with water gives an emulsion, whereby a formulation with 25% (w/w) of active compound(s) is obtained.

E) Suspensions (SC, OD, FS)

In an agitated ball mill, 20 parts by weight of the active compound(s) are comminuted with addition of 10 parts by weight of dispersants, wetters and 70 parts by weight of water or of an organic solvent to give a fine active compound(s) suspension. Dilution with water gives a stable suspension of the active compound(s), whereby a formulation with 20% (w/w) of active compound(s) is obtained.

F) Water-Dispersible Granules and Water-Soluble Granules (WG, SG)

50 parts by weight of the active compound(s) are ground finely with addition of 50 parts by weight of dispersants and wetters and made as water-dispersible or water-soluble granules by means of technical appliances (for example extrusion, spray tower, fluidized bed). Dilution with water gives a stable dispersion or solution of the active cornpound(s), whereby a formulation with 50% (w/w) of active compound(s) is obtained.

G) Water-Dispersible Powders and Water-Soluble Powders (WP, SP, SS, WS)

75 parts by weight of the active compound(s) are ground in a rotor-stator mill with addition of 25 parts by weight of dispersants, wetters and silica gel. Dilution with water gives a stable dispersion or solution of the active compound(s), whereby a formulation with 75% (w/w) of active compound(s) is obtained.

2. Products to be applied undiluted for foliar applications. For seed treatment purposes, such products may be applied to the seed diluted or undiluted.

H) Dustable Powders (DP, DS)

5 parts by weight of the active compound(s) are ground finely and mixed intimately with 95 parts by weight of finely divided kaolin. This gives a dustable product having 5% (w/w) of active compound(s)

I) Granules (GR, FG, GG, MG)

0.5 part by weight of the active compound(s) is ground finely and associated with 95.5 parts by weight of carriers, whereby a formulation with 0.5% (w/w) of active compound(s) is obtained. Current methods are extrusion, spray-drying or the fluidized bed. This gives granules to be applied undiluted for foliar use.

J) ULV Solutions (UL, LS)

10 parts by weight of the active compound(s) are dissolved in 90 parts by weight of an organic solvent, for example xylene. This gives a product having 10% (w/w) of active compound(s), which is applied undiluted for foliar use.

Various types of oils, wetters, adjuvants, herbicides, fungicides, other pesticides, or bactericides may be added to the active ingredients, if appropriate just immediately prior to use (tank mix). These agents usually are admixed with the agents according to the invention in a weight ratio of 1:10 to 10:1.

The compounds of formula I are effective through both contact and ingestion.

The compounds of formula I are also suitable for the protection of the seed, plant propagules and the seedlings' roots and shoots, preferably the seeds, against soil pests and also for the treatment plant seeds which tolerate the action of herbicides or fungicides or insecticides owing to breeding, including genetic engineering methods.

Conventional seed treatment formulations include for example flowable concentrates FS, solutions LS, powders for dry treatment DS, water dispersible powders WS or granules for slurry treatment, water soluble powders SS and emulsion ES. Application to the seeds is carried out before sowing, either directly on the seeds.

The seed treatment application of the compounds of formula I or formulations containing them is carried out by spraying or dusting the seeds before sowing of the plants and before emergence of the plants.

The invention also relates to the propagation product of plants, and especially the treated seed comprising, that is, coated with and/or containing, a compound of formula I or a composition comprising it. The term “coated with and/or containing” generally signifies that the active ingredient is for the most part on the surface of the propagation product at the time of application, although a greater or lesser part of the ingredient may penetrate into the propagation product, depending on the method of application. When the said propagation product is (re)planted, it may absorb the active ingredient. The seed comprises the inventive compounds or compositions comprising them in an amount of from 0,1 g to 10 kg per 100 kg of seed.

Compositions of this invention may also contain other active ingredients, for example other pesticides, insecticides, herbicides, fertilizers such as ammonium nitrate, urea, potash, and superphosphate, phytotoxicants and plant growth regulators, safeners and nematicides. These additional ingredients may be used sequentially or in combination with the above-described compositions, if appropriate also added only immediately prior to use (tank mix). For example, the plant(s) may be sprayed with a composition of this invention either before or after being treated with other active ingredients.

The following list of pesticides together with which the compounds according to the invention can be used, is intended to illustrate the possible combinations, but not to impose any limitation:

A.1. Organo(thio)phosphates: acephate, azamethiphos, azinphos-methyl, chlorpyrifos, chlorpyrifos-methyl, chlorfenvinphos, diazinon, dichlorvos, dicrotophos, dimethoate, disulfoton, ethion, fenitrothion, fenthion, isoxathion, malathion, methamidophos, methidathion, methyl-parathion, mevinphos, monocrotophos, oxydemeton-methyl, paraoxon, parathion, phenthoate, phosalone, phosmet, phosphamidon, phorate, phoxim, pirimi-phos-methyl, profenofos, prothiofos, sulprophos, tetrachlorvinphos, terbufos, triazophos, trichlorfon; A.2. Carbamates: alanycarb, aldicarb, bendiocarb, benfuracarb, carbaryl, carbofuran, carbosulfan, fenoxycarb, furathiocarb, methiocarb, methomyl, oxamyl, pirimicarb, propoxur, thiodicarb, triazamate; A.3. Pyrethroids: allethrin, bifenthrin, cyfluthrin, cyhalothrin, cyphenothrin, cypermethrin, alpha-cypermethrin, beta-cypermethrin, zeta-cypermethrin, deltamethrin, esfenvalerate, etofenprox, fenpropathrin, fenvalerate, imiprothrin, lambda-cyhalothrin, permethrin, prallethrin, pyrethrin I and II, resmethrin, silafluofen, tau-fluvalinate, tefluthrin, tetramethrin, tralomethrin, transfluthrin; A.4. Growth regulators: a) chitin synthesis inhibitors: benzoylureas: chlorfluazuron, cyramazin, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, teflubenzuron, triflumuron; buprofezin, diofenolan, hexythiazox, etoxazole, clofentazine; b) ecdysone antagonists: halofenozide, methoxyfenozide, tebufenozide, azadirachtin; c) juvenoids: pyriproxyfen, methoprene, fenoxycarb; d) lipid biosynthesis inhibitors: spirodiclofen, spiromesifen, a tetronic acid derivative of formula Γ¹,

A.5. Nicotinic receptor agonists/antagonists compounds: clothianidin, dinotefuran, imidacloprid, thiamethoxam, nitenpyram, acetamiprid, thiacloprid; A.6. GABA antagonist compounds: acetoprole, endosulfan, ethiprole, fipronil, vaniliprole; A.7. Macrocyclic lactone insecticides: abamectin, emamectin, milbemectin, lepimectin, spinosad; A.8. METI I acaricides: fenazaquin, pyridaben, tebufenpyrad, tolfenpyrad; A.9. METI II and III compounds: acequinocyl, fluacyprim, hydramethylnon; A.10. Uncoupler compounds: chlorfenapyr; A.11. Oxidative phosphorylation inhibitor compounds: cyhexatin, diafenthiuron, fenbutatin oxide, propargite; A.12. Moulting disruptor compounds: cryomazine; A.13. Mixed Function Oxidase inhibitor compounds: piperonyl butoxide; A.14. Sodium channel blocker compounds: indoxacarb, metaflumizone; A.15. Various: benclothiaz, bifenazate, cartap, flonicamid, pyridalyl, pymetrozine, sulfur, thiocyclam, N—R′-2,2-dihalo-1-R″cyclo-propanecarboxamide-2-(2,6-dichloro-α,α,α-trifluoro-p-tolyl)hydrazone or N—R′-2,2-di(R′″)propionamide-2-(2,6-dichloro-α,α,α-trifluoro-p-tolyl)-hydrazone, wherein R′″ is methyl or ethyl, halo is chloro or bromo, R″ is hydrogen or methyl and R′″ is methyl or ethyl, and the aminoisothiazole compounds of formula Γ²,

wherein R^(i) is —CH₂OCH₂CH₃ or H and R^(ii) is CF₂CF₂CF₃ or CH₂CH(CH₃)₃, anthranilamide compounds of formula Γ³

wherein B¹ is hydrogen or a chlorine atom, B² is a bromine atom or CF₃, and R^(B) is CH₃ or CH(CH₃)₂, and malononitrile compounds as described in JP 2002 284608, WO 02/89579, WO 02/90320, WO 02/90321, WO 04/06677, WO 04/20399, or JP 2004 99597.

The insects may be controlled by contacting the target parasite/pest, its food supply, habitat, breeding ground or its locus with a pesticidally effective amount of compounds of or compositions of formula I.

“Locus” means a habitat, breeding ground, plant, seed, soil, area, material or environment in which a pest or parasite is growing or may grow.

In general, “pesticidally effective amount” means the amount of active ingredient needed to achieve an observable effect on growth, including the effects of necrosis, death, retardation, prevention, and removal, destruction, or otherwise diminishing the occurrence and activity of the target organism. The pesticidally effective amount can vary for the various compounds/compositions used in the invention. A pesticidally effective amount of the compositions will also vary according to the prevailing conditions such as desired pesticidal effect and duration, weather, target species, locus, mode of application, and the like.

The compounds or compositions of the invention can also be applied preventively to places at which occurrence of the pests is expected.

The compounds of formula I may also be used to protect growing plants from attack or infestation by pests by contacting the plant with a pesticidally effective amount of compounds of formula I. As such, “contacting” includes both direct contact (applying the compounds/compositions directly on the pest and/or plant—typically to the foliage, stem or roots of the plant) and indirect contact (applying the compounds/compositions to the locus of the pest and/or plant).

In the case of soil treatment or of application to the pests dwelling place or nest, the quantity of active ingredient ranges from 0.0001 to 500 g per 100 m², preferably from 0.001 to 20 g per 100 m².

For use in treating crop plants, the rate of application of the active ingredients of this invention may be in the range of 0.1 g to 4000 g per hectare, desirably from 25 g to 600 g per hectare, more desirably from 50 g to 500 g per hectare.

Compounds of formula I and compositions comprising them can also be used for controlling and preventing infestations and infections in animals including warm-blooded animals (including humans) and fish. They are for example suitable for controlling and preventing infestations and infections in mammals such as cattle, sheep, swine, camels, deer, horses, pigs, poultry, rabbits, goats, dogs and cats, water buffalo, donkeys, fallow deer and reindeer, and also in fur-bearing animals such as mink, chinchilla and raccoon, birds such as hens, geese, turkeys and ducks and fish such as fresh- and salt-water fish such as trout, carp and eels.

Infestations in warm-blooded animals and fish include, but are not limited to, lice, biting lice, ticks, nasal bots, keds, biting flies, muscoid flies, flies, myiasitic fly larvae, chiggers, gnats, mosquitoes and fleas.

The compounds of formula I and compositions comprising them are suitable for systemic and/or non-systemic control of ecto- and/or endoparasites. They are active against all or some stages of development.

Administration can be carried out both prophylactically and therapeutically. Administration of the active compounds is carried out directly or in the form of suitable preparations, orally, topically/dermally or parenterally.

For oral administration to warm-blooded animals, the formula I compounds may be formulated as animal feeds, animal feed premixes, animal feed concentrates, pills, solutions, pastes, suspensions, drenches, gels, tablets, boluses and capsules. In addition, the formula I compounds may be administered to the animals in their drinking water. For oral administration, the dosage form chosen should provide the animal with 0.01 mg/kg to 100 mg/kg of animal body weight per day of the formula I compound, preferably with 0.5 mg/kg to 100 mg/kg of animal body weight per day.

Alternatively, the formula I compounds may be administered to animals parenterally, for example, by intraruminal, intramuscular, intravenous or subcutaneous injection. The formula I compounds may be dispersed or dissolved in a physiologically acceptable carrier for subcutaneous injection. Alternatively, the formula I compounds may be formulated into an implant for subcutaneous administration. In addition the formula I compound may be transdermally administered to animals. For parenteral administration, the dosage form chosen should provide the animal with 0.01 mg/kg to 100 mg/kg of animal body weight per day of the formula I compound.

The formula I compounds may also be applied topically to the animals in the form of dips, dusts, powders, collars, medallions, sprays, shampoos, spot-on and pour-on formulations and in ointments or oil-in-water or water-in-oil emulsions. For topical application, dips and sprays usually contain 0.5 ppm to 5,000 ppm and preferably 1 ppm to 3,000 ppm of the formula I compound. In addition, the formula I compounds may be formulated as ear tags for animals, particularly quadrupeds such as cattle and sheep.

Suitable preparations are:

-   -   Solutions such as oral solutions, concentrates for oral         administration after dilution, solutions for use on the skin or         in body cavities, pouring-on formulations, gels;     -   Emulsions and suspensions for oral or dermal administration;         semi-solid preparations;     -   Formulations in which the active compound is processed in an         ointment base or in an oil-in-water or water-in-oil emulsion         base;     -   Solid preparations such as powders, premixes or concentrates,         granules, pellets, tablets, boluses, capsules; aerosols and         inhalants, and active compound-containing shaped articles.

Generally it is favorable to apply solid formulations which release compounds of formula I in total amounts of 10 mg/kg to 300 mg/kg, preferably 20 mg/kg to 200 mg/kg. The active compounds can also be used as a mixture with synergists or with other active compounds which act against pathogenic endo- and ectoparasites.

In general, the compounds of formula I are applied in parasiticidally effective amount-meaning the amount of active ingredient needed to achieve an observable effect on growth, including the effects of necrosis, death, retardation, prevention, and removal, destruction, or otherwise diminishing the occurrence and activity of the target organism. The parasiticidally effective amount can vary for the various compounds/compositions used in the invention. A parasiticidally effective amount of the compositions will also vary according to the prevailing conditions such as desired parasiticidal effect and duration, target species, mode of application, and the like.

SYNTHESIS EXAMPLES

With due modification of the starting compounds, the protocols shown in the synthesis examples below were used for obtaining further compounds I. The resulting compounds, together with physical data, are listed in the Tables 1 to 3 which follow.

2-[5-Bromo-2-(3-chloro-pyridin-2-yl)-2H-pyrazol-3-yl]-8-methyl-benzo[d][1,3]oxazin-4-one is known from WO 04/011447.

Example 1 Methyl-phenyl-sulfamoyl-N-(5-bromo-2-(3-chloro-pyridin-2-yl)-2H-pyrazole-3-carboxylic acid (2-carbamoyl-6-methyl-phenyl))-amide, compound I.1-33

0.089 g Methyl-phenyl-sulfamoyl-amine was dissolved in 5 ml methylene chloride. 0.017 g sodium hydride was added at 20-25° C. and the solution was stirred for 1 hour. 0.20 g 2-[5-Bromo-2-(3-chloro-pyridin-2-yl)-2H-pyrazol-3-yl]-8-methyl-benzo[d][1,3]oxazin-4-one were added and the resulting mixture was refluxed for 24 h. The solvent was removed and the residue was purified by column chromatography (cyclo hexane/ethyl acetate 1:2) to yield 0.18 g methyl-phenyl-sulfamoyl-N-(5-bromo-2-(3-chloropyridin-2-yl)-2H-pyrazole-3-carboxylic acid (2-carbamoyl-6-methyl-phenyl))-amide

Example 2 Step A: Preparation of 5-bromo-2-(3-chloro-pyridin-2-yl)-2H-pyrazole-3-carboxylic acid (2-carbamoyl-6-methyl-phenyl)-amide

1.00 g 2-[5-Bromo-2-(3-chloro-pyridin-2-yl)-2H-pyrazol-3-yl]-8-methyl-benzo[d][1,3]oxazin-4-one was taken up in 10 ml of a 25% ammonia solution in water and stirred for 72 h. The solids were filtered and washed with cold water to yield 0.80 g of the amide.

Step B: S,S-Dimethyl-N-(5-bromo-2-(3-chloro-pyridin-2-yl)-2H-pyrazole-3-carboxylic acid (2-carbamoyl-6-methyl-phenyl))-sulfimide, compound I.3-2.

0.071 ml DMSO were dissolved under a nitrogen atmosphere in 0.5 ml methylene chloride and cooled to −60° C. 0.14 ml trifluoroacetic acid anhydride were slowly added at this temperature followed by the addition of 0.20 g 5-bromo-2-(3-chloro-pyridin-2-yl)-2H-pyrazole-3-carboxylic acid (2-carbamoyl-6-methyl-phenyl)-amide. The resulting solution was stirred at −35° C. for 1 h. After diluting with 5 ml methylene chloride, the reaction mixture was extracted with aqueous sodium hydroxide once and two times with water. The organic solvent was dried and the solvent removed. The residue was diluted with diethyl ether and the solid residue was filtered off and dried to yield 0.08 g of the desired sulfimide.

Example 3

S,S Dimethyl-S— Aminosulfonium mesitylenesulfonate was prepared according to Y. Tamura et al, Tetrahedron, 1975, 31, 3035-3040.

S,S-Dimethyl-N-(5-bromo-2-(3-chloro-pyridin-2-yl)-2H-pyrazole-3-carboxylic acid (2-carbamoyl-6-methyl-phenyl))-sulfimide, compound I.3-2.

0.2 g S,S Dimethyl-S— Aminosulfonium mesitylenesulfonate were dissolved in 20 ml methylene chloride. 0.26 g potassium t-butylate, 0.54 g 2-[5-Bromo-2-(3-chloro-pyridin-2-yl)-2H-pyrazol-3-yl]-8-methyl-benzo[d][1,3]oxazin-4-one were added and the resulting mixture was stirred at 20-25° C. for additional 3.5 h. The reaction mixture was extracted with aqueous sodium hydroxide once and two times with water. The organic solvent was dried and the solvent removed. Column chromatography yielded 0.3 g of the desired product.

Example 4 2-{2-[5-Bromo-2-(2-chloro-phenyl)-2H-pyrazol-3-yl]-2-oxo-ethyl}-5-chloro-3-methyl-N-(1-oxo-hexahydro-1lambda*6*-thiopyran-1-ylidene)-benzamide

0.2 g 2-{2-[5-Bromo-2-(2-chloro-phenyl)-2H-pyrazol-3-yl]-2-oxo-ethyl}-5-chloro-3-methyl-N-(tetrahydro-1lambda*4*-thiopyran-1-ylidene)-benzamide (0.35 mmol) were dissolved in 10 ml acetic acid. 4 mg Sodium wolframate dihydrate were added. 45 mg of a 30% solution of hydrogenperoxide was added dropwise and the resulting solution was stirred for 18 h. The reaction mixture was poured into a saturated aqueous sodium carbonate solution, methylene chloride was added and the organic pase was subsequently washed with water and saturated aqueous sodium carbonate. The organic solvent was dried and the solvent removed. Column chromatography yielded 0.07 g of the desired product, compound I.4-22.

The products were characterized by coupled High Performance Liquid Chromatography/mass spectrometry (HPLC/MS), by NMR or by their melting points.

TABLE I (I.1)

Physical Data: Meltingpoint [° C.] No. Q¹ Q³ R¹² R¹³ ¹H-NMR, δ [ppm] I.1-1 Cl Br CH₂CH₃ i-C₃H₇ >210  I.1-2 Cl Br CH₂CH₃ c-C₆H₁₁ 191 I.1-3 Cl Br i-C₃H₇ i-C₃H₇ 150-151 I.1-4 Cl Br i-CH₃H₇ CH₂CHCH₂ >210  I.1-5 Cl Br CH₃ CH₂CCH 162-163 I.1-6 Cl Br CH₃ CH₂CHCH₂ 123 I.1-7 Cl Br CH₃ CH₂CH₃   102.20 I.1-8 Cl Br CH₃ i-CH₃H₇ 200 I.1-9 Cl Br CH₃ CH₃ 203 I.1-10 Cl Br CH₃ c-C₆H₁₁ 176-177 I.1-11 Cl Br CH₃ CH₂C₆H₅ 154-155 I.1-12 Cl Br CH₃ C₆H₅ 155-156 I.1-13 Cl Br CH₃ i-C₄H₉ 148-149 I.1-14 Cl Br CH₃ CH₂CH₂C₆H₅ 167-168 I.1-15 Cl Br n-C₃H₇ i-C₃H₇ >210  I.1-16 Cl Br n-C₃H₇ CH₂CH₂OMe 150-151 I.1-17 H Br CH₂CH₃ c-C₆H₁₁ 191 I.1-18 H Br CH₂CH₃ CH₂CH₃ 191 I.1-19 H Br CH₂CH₃ i-C₃H₇ 209 I.1-20 H Br i-C₃H₇ CH₂CHCH₂ 185 I.1-21 H Br i-C₃H₇ n-C₃H₇ 204 I.1-22 H Br i-C₃H₇ i-C₃H₇ 151 I.1-23 H Br CH₃ CH₂CHCH₂ 153 I.1-24 H Br CH₃ CH₂C₆H₅ 2.3(s), 2.6(s), 4.2(s), 7.2-7.7(m), 8.1(d), 8.4(d), 10.3(s), 11.9(s) [d₆-DMSO] I.1-25 H Br CH₃ CH₂CCH 172 I.1-26 H Br CH₃ CH₂CH₂C₆H₅ 178 I.1-27 H Br CH₃ CH₂CH₃ 202 I.1-28 H Br CH₃ i-C₄H₉ 0.8(d), 1.8(m), 2.2(s), 2.6(s), 2.8(s), 7.2-7.6(m), 8.1(d), 8.5(d), 10.2(s), 11.7(s) [d₆-DMSO] I.1-29 H Br CH₃ i-C₃H₇ 1.0(d), 2.2(s), 2.8(s), 4.3(m), 7.2-7.4(m), 7.8(d), 8.4(d), 8.6(s), 9.6(s) [CDCl₃] I.1-30 H Br CH₃ CH₃ 205 I.1-31 H Br CH₃ n-C₃H₇ 203 I.1-32 H Br CH₃ C₆H₅ 1.0(d), 2.1(s), 7.2-7.7(m), 8.1(d), 8.4(d), 10.3(s), 11.9(s) [d₆-DMSO] I.1-33 H Br CH₃ C₆H₅ 199 I.1-34 Cl CF₃ CH₂CH₂OMe CH₂CH₂CH₃ 150 I.1-35 Cl CF₃ CH₂CHCH₂ i-C₃H₇ 190 I.1-36 Cl CF₃ CH₂CH₃ c-C₆H₁₁ 185 I.1-37 Cl CF₃ CH₂CH₃ CH₂CH₃ >240  I.1-38 Cl CF₃ CH₂CH₃ i-C₃H₇ 155 I.1-39 Cl CF₃ i-C₃H₇ i-C₃H₇ 180 I.1-40 Cl CF₃ i-C₃H₇ n-C₃H₇ 175 I.1-41 Cl CF₃ CH₃ CH₂CCH 155 I.1-42 Cl CF₃ CH₃ CH₂CH₂Ph 160 I.1-43 Cl CF₃ CH₃ CH₂CHCH₂  90 I.1-44 Cl CF₃ CH₃ c-C₆H₁₁ 102 I.1-45 Cl CF₃ CH₃ CH₂CH₃ 110 I.1-46 Cl CF₃ CH₃ i-C₄H₉ 160 I.1-47 Cl CF₃ CH₃ CH₃ 198 I.1-48 Cl CF₃ CH₃ CH₂C₆H₅ 120 I.1-49 Cl CF₃ CH₃ C₆H₅ 130 I.1-50 Cl CF₃ CH₂CH₂OMe n-C₃H₇ 180 I.1-51 Cl CF₃ CH₂CHCH₂ i-C₃H₇ 177 I.1-52 Cl CF₃ CH₂CH₃ c-C₆H₁₁ 200 I.1-53 Cl CF₃ CH₂CH₃ CH₂CH₃ 180 I.1-54 Cl CF₃ i-C₃H₇ i-C₃H₇ 190 I.1-55 Cl CF₃ i-C₃H₇ n-C₃H₇ 185 I.1-56 Cl CF₃ CH₃ CH₂C₆H₅ 165 I.1-57 H CF₃ CH₃ CH₂CCH 165 I.1-58 H CF₃ CH₃ CH₂CH₂C₆H₅ 165 I.1-59 H CF₃ CH₃ CH₂CHCH₂ 160 I.1-60 H CF₃ CH₃ c-C₆H₁₁ 205 I.1-61 H CF₃ CH₃ CH₂CH₃ 195 I.1-62 H CF₃ CH₃ i-C₄H₉ 175 I.1-63 H CF₃ CH₃ i-C₃H₇ 1.1(d), 2.2(s), 2.8(s), 4.3(m), 7.2-7.5(m), 7.9(d), 8.5(d), 8.6(s), 9.7(s) [CDCl₃] I.1-64 H CF₃ CH₃ CH₃ 183 I.1-65 H CF₃ CH₃ C₆H₅ 115 I.1-66 Cl CF₃ n-C₃H₇

140 I.1-67 H CF₃ n-C₃H₇

195 I.1-68 H Br n-C₃H₇

199 I.1-69 Cl Br n-C₃H₇

159-160

TABLE II (I.2)

Physical Data Melting Point [° C.] No. Q¹ Q³ R⁴ ¹H-NMR, δ [ppm] I.2-1 Cl CF₃

115 I.2-2 Cl CF₃

160 I.2-3 Cl CF₃

145 I.2-4 Cl CF₃

115 I.2-5 Cl Br

105-106 I.2-6 Cl Br

138-139 I.2-7 H CF₃

175 I.2-8 H CF₃

182 I.2-9 H CF₃

150 I.2-10 Cl Br

oil I.2-11 Cl Br

135 I.2-12 H Br

162 I.2-13 H Br

151 I.2-14 H Br

162 I.2-15 H Br

150 I.2-16 Cl CF₃

198 I.2-17 H CF₃

190 I.2-18 H CF₃

165 *denotes the binding site

TABLE III (I.3)

Melting Point No. Q¹ Q³ R² R³ [° C.] I.3-1 Cl CF₃ i-C₃H₇ i-C₃H₇ 163 I.3-2 H Br CH₃ CH₃ 165 I.3-3 Cl Br CH₂CH₃ CH₂CH₃ oil I.3-4 Cl Br CH₃ CH₃ 185 I.3-5 Cl Br i-C₃H7 i-CH₃H₇ 165 decomp. I.3-6 Cl CF₃ i-C₃H₇ i-C₃H₇ 142 I.3-7 H Br CH₃ CH₃ 200 I.3-8 Cl CF₃ CH₃ CH₃ 182 I.3-9 H Br n-C₃H₇ CH₃ 150 I.3-10 H CF₃ n-C₃H₇ CH₃ 143 I.3-11 Cl Br n-C₃H₇ CH₃ 179 I.3-12 Cl Br n-C₅H₁₁ CH₂CH₂OH 160 I.3-13 H Br n-C₅H₁₁ CH₂CH₂OH  70 decomp. I.3-14 Cl CF₃ CH₃ n-C₃H₇  60 decomp. I.3-15 I CF₃ CH₃ n-C₃H₇  85 I.3-16 I Br CH₃ n-C₃H₇ 180 decomp. I.3-17 H CF₃ n-C₅H₁₁ CH₂CH₂OH 106 I.3-18 I Br n-C₅H₁₁ CH₂CH₂OH 150 decomp. I.3-19 I Br i-C₃H₇ i-C₃H₇  75 I.3-20 I CF₃ i-C₃H₇ i-C₃H₇  75 I.3-21 H Br i-C₃H₇ i-C₃H₇ 180 I.3-22 I Br CH₃ CH₃ 115 I.3-23 I CF₃ CH₃ CH₃ 165 I.3-24 H CF₃ CH₃ CH₃ 206 I.3-25 Cl Br CH₂CH₃ CH₃ 192 I.3-26 H Br CH₂CH₃ CH₃ 161 I.3-27 I Br CH₂CH₃ CH₃ 124 I.3-28 Cl CF₃ CH₂CH₃ CH₃ 181 I.3-29 H CF₃ CH₃ CH₂CH₃ 181 I.3-30 I CF₃ CH₂CH₃ CH₃ 181 I.3-31 H CF₃ i-C₃H₇ i-C₃H₇ 192 I.3-32 Cl CF₃ n-C₅H₁₁ CH₂CH₂OH 133 I.3-33 I CF₃ n-C₅H₇ CH₂CH₂OH 135 I.3-34 Cl CF₃ CH₃ p-F—C₆H₄ 185 I.3-35 Cl Br CH₃ p-F—C₆H₄ 195 I.3-36 H Br CH₃ p-F—C₆H₄ 120 I.3-37 H CF₃ CH₃ p-F—C₆H₄ 180 I.3-38 I CF₃ CH₃ p-F—C₆H₄ 182 I.3-39 I Br CH₃ p-F—C_(6l H) ₄ 201 I.3-40 Cl Br CH₂CH₂Cl CH₂CH₃ 158 I.3-41 Cl Br CH₂CH₃ CHCH₂  75 I.3-42 H Br CH₂CH₃ CHCH₂  60 I.3-43 I Br CH₂CH₃ CHCH₂  80 I.3-44 I Br CH₂CH₂Cl CH₂CH₃  80 I.3-45 Cl OCH₂CCH i-C₃H₇ i-C₃H₇ oil I.3-46 I OCH₂CCH i-C₃H₇ i-C₃H₇ oil I.3-47 Cl OCH₂CCH CH₃ p-F—C₆H₄ oil I.3-48 I OCH₂CCH CH₃ p-F—C₆H₄ oil I.3-49 Cl OCH₂CCH CH₂CH₂OH n-C₅H₁₁ oil I.3-50 I OCH₂CCH CH₂CH₂OH n-C₅H₁₁ oil I.3-51 H CF₃ CH₂CH₃ CH₂CH₂Cl 171 I.3-52 I CF₃ CH₂CH₂Cl CH₂CH₃ 164 I.3-53 CN CF₃ n-C₃H₇ CH₃  70 I.3-54 CN CF₃ p-F—C₆H₄ CH₃  72 I.3-55 CN CF₃ CH₃ CH₃ 225 I.3-56 CN Br n-C₃H₇ CH₃  70 I.3-57 CN Br p-F—C₆H₄ CH₃ 180 I.3-58 CN Br n-C₅H₇ CH₂CH₂OH  50 I.3-59 CN Br i-C₃H₇ i-C₃H₇ 185 I.3-60 CN Br CH₃ CH₃ 205 I.3-61 CN Br CH₂CH₃ CH₃  80 I.3-62 CN Br CH₂CH₃ CHCH₂  60 I.3-63 CN Br CH₃ s-C₄H₉  71 I.3-64 CN CF₃ CH₂CH₃ CHCH₂  60 I.3-65 CN CF₃ CH₃ CH₂CH₃  65 I.3-66 CN CF₃ CH₂CH₂OH n-C₅H₁₁  47 I.3-67 CN CF₃ s-C₄H₉ CH₃  66 I.3-68 CN CF₃ i-C₃H₇ i-C₃H₇ 131 ″decomp.″ denotes the onset temperature of the decomposition.

TABLE IV (I.4)

No. Q¹ Q³

Physical Data: Meltingpoint [° C.] I.4-1 Cl Br

203 I.4-2 I Br

195 I.4-3 I CF₃

185 I.4-4 H CF₃

208 I.4-5 Cl CF₃

182 I.4-6 Cl Br

165 I.4-7 I Br

120 I.4-8 H CF₃

188 I.4-9 H Br

169 I.4-10 I CF₃

148 I.4-11 I CF₃

215 I.4-12 Cl Br

203 I.4-13 I Br

213 I.4-14 Cl OCH₂CCH

Oil I.4-15 Cl OCH₂CCH

Oil I.4-16 CN CF₃

 85 I.4-17 CN Br

 92 I.4-18 CN Br

 85 I.4-19 CN Br

 85 I.4-20 CN CF₃

 88 I.4-21 CN CF₃

194 I.4-22 Cl Br

Oil I.4-23 Cl CF₃ [CH₂CH₂OH] oil [(CH₂)₄CH₃]S(═O)— Examples for the Action Against Harmful Pests 1. Activity Against Boll Weevil (Anthonomus grandis)

The active compounds were formulated in 1:3 DMSO:water. 10 to 15 eggs were placed into microtiterplates filled with 2% agar-agar in water and 300 ppm formaline. The eggs were sprayed with 20 μl of the test solution, the plates were sealed with pierced foils and kept at 24-26° C. and 75-85% humidity with a day/night cycle for 3 to 5 days. Mortality was assessed on the basis of the remaining unhatched eggs or larvae on the agar surface and/or quantity and depth of the digging channels caused by the hatched larvae. Tests were replicated 2 times.

In this test, compounds I.1-3, I.1-11, I.1-15, I.1-32, I.1-35, I.1-48, I.1-69, I.2-2, I.3-1, I.3-3, I.3-4, I.3-5, I.3-6, I.3-7, I.3-8, I.3-9, I.3-10, I.3-11, I.3-12, I.3-13, I.3-14, I.3-19, I.3-20, I.3-21, I.3-22, I.3-23, I.3-24, I.3-25, I.3-26, I.3-27, I.3-28, I.3-29, I.3-30, I.3-31, I.3-32, I.3-33, I.3-34, I.3-35, I.3-36, I.3-37, I.3-38, I.3-39, I.3-40, I.3-41, I.3-42, I.3-43, I.3-44, I.3-45, I.3-46, I.3-47, I.3-48, I.3-49, I.3-51, I.3-52, I.3-53, I.3-54, I.3-55, I.3-56, I.3-57, I.3-58, I.4-1, I.4-2, I.4-3, I.4-4, I.4-5, I.4-6, I.4-7, I.4-8, I.4-9, I.4-10, I.4-11, I.4-12, I.4-13, I.4-14, I.4-15, I.4-16, I.4-17, I.4-22, and I.4-23 at 2500 ppm showed over 75% mortality.

2. Activity Against Mediterranean Fruitfly (Ceratitis capitata)

The active compounds were formulated in 1:3 DMSO:water. 50 to 80 eggs were placed into microtiterplates filled with 0.5% agar-agar and 14% diet in water. The eggs were sprayed with 5 μl of the test solution, the plates were sealed with pierced foils and kept at 27-29° C. and 75-85% humidity under fluorescent light for 6 days. Mortality was assessed on the basis of the agility of the hatched larvae. Tests were replicated 2 times.

In this test, compounds I.1-12, I.1-38, I.1-43, I.1-44, I.1-49, I.3-1, I.3-8, I.3-9, I.3-10, I.3-11, I.3-12, I.3-13, I.3-14, I.3-19, I.3-20, I.3-22, I.3-23, I.3-24, I.3-25, I.3-26, I.3-27, I.3-28, I.3-29, I.3-30, I.3-32, I.3-33, I.3-34, I.3-35, I.3-37, I.3-38, I.3-39, I.3-40, I.3-41, I.3-42, I.3-43, I.3-44, I.3-45, I.3-46, I.3-47, I.3-48, I.3-49, I.3-51, I.3-52, I.3-53, I.3-54, I.3-55, I.3-56, I.3-57, I.3-58, I.4-1, I.4-2, I.4-3, I.4-4, I.4-5, I.4-6, I.4-7, I.4-8, I.4-9, I.4-10, I.4-11, I.4-12, I.4-13, I.4-15, I.4-16, I.4-17, I.4-22 and I.4-23 at 2500 ppm showed over 75% mortality.

3. Activity Against Tobacco Budworm (Hellothis virescens)

The active compounds were formulated in 1:3 DMSO:water. 15 to 25 eggs were placed into microtiterplates filled with diet. The eggs were sprayed with 10μl of the test solution, the plates were sealed with pierced foils and kept at 27-29° C. and 75-85% humidity under fluorescent light for 6 days. Mortality was assessed on the basis of the agility and of comparative feeding of the hatched larvae. Tests were replicated 2 times.

-   4. In this test, compounds I.1-1, I.1-3, I.1-10, I.1-11, I.1-12,     I.1-13, I.1-14, I.1-15, I.1-16, I.1-19, I.1-21, I.1-24, I.1-28,     I.1-31, I.1-32, I.1-34, I.1-35, I.1-36, I.1-38, I.1-39, I.1-40,     I.1-41, I.1-42, I.1-43, I.1-44, I.1-46, I.1-48, I.1-49, I.1-53,     I.1-54, I.1-62, I.1-66, I.1-67, I.1-69, I.2-1, I.2-2, I.2-3, I.2-4,     I.2-5, I.2-6, I.3-1, I.3-3, I.3-4, I.3-5, I.3-6, I.3-7, I.3-8,     I.3-9, I.3-10, I.3-11, I.3-12, I.3-13, I.3-14, I.3-19, I.3-20,     I.3-21, I.3-22, I.3-23, I.3-24, I.3-25, I.3-26, I.3-27, I.3-28,     I.3-29, I.3-30, I.3-31, I.3-32, I.3-33, I.3-34, I.3-35, I.3-36,     I.3-37, I.3-38, I.3-39, I.3-40, I.3-41, I.3-42, I.3-43, I.3-44,     I.3-45, I.3-46, I.3-47, I.3-48, I.3-49, I.3-51, I.3-52, I.3-53,     I.3-54, I.3-55, I.3-56, I.3-57, I.3-58, I.4-1, I.4-2, I.4-3, I.4-4,     I.4-5, I.4-6, I.4-7, I.4-8, I.4-9, I.4-10, I.4-11, I.4-12, I.4-13,     I.4-14, I.4-15, I.4-16, I.4-17, I.4-22 and I.4-23 at 2500 ppm showed     over 75% mortality.     4. Activity Against Vetch Aphid (Megoura viciae)

The active compounds were formulated in 1:3 DMSO:water. Bean leaf disks were placed into microtiterplates filled with 0.8% agar-agar and 2.5 ppm OPUS™. The leaf disks were sprayed with 2.5 μl of the test solution and 5 to 8 adult aphids were placed into the microtiterplates which were then closed and kept at 22-24° C. and 35-45% under fluorescent light for 6 days. Mortality was assessed on the basis of vital, reproduced aphids. Tests were replicated 2 times.

In this test, compounds I.1-12, I.1-19, I.1-32, I.1-49, I.1-50, I.1-53, I.2-9, I.3-1, I.3-3, I.3-4, I.3-5, I.3-6, I.3-7, I.3-8, I.3-9, I.3-10, I.3-11, I.3-12, I.3-13, I.3-14, I.3-19, I.3-20, I.3-21, I.3-22, I.3-23, I.3-24, I.3-25, I.3-26, I.3-27, I.3-28, I.3-29, I.3-30, I.3-32, I.3-33, I.3-34, I.3-35, I.3-36, I.3-37, I.3-38, I.3-39, I.3-40, I.3-41, I.3-42, I.3-43, I.3-44, I.3-45, I.3-47, I.3-49, I.3-51, I.3-52, I.3-53, I.3-54, I.3-55, I.3-56, I.3-57, I.3-58, I.4-1, I.4-2, I.4-3, I.4-4, I.4-5, I.4-6, I.4-7, I.4-8, I.4-9, I.4-10, I.4-11, I.4-12, I.4-13, I.4-14, I.4-15, I.4-16, I.4-17, I.4-22 and I.4-23 at 2500 ppm showed over 75% mortality compared to 0% mortality of untreated controls.

5. Activity Against Oat Aphid (Rhopalosiphum padi)

The active compounds were formulated in 1:3 DMSO:water. Barlay leaf disk were placed into microtiterplates filled with 0.8% agar-agar and 2.5 ppm OPUS™. The leaf disks were sprayed with 2.5 μl of the test solution and 3 to 8 adult aphids were placed into the microtiterplates which were then closed and kept at 22-24° C. and 35-45% humidity under fluorescent light for 5 days. Mortality was assessed on the basis of vital aphids. Tests were replicated 2 times.

In this test, compound I.3-1 at 2500 ppm showed over 75% mortality compared to 0% mortality of untreated controls.

6. Activity Against Cotton Aphid (Aphis gossypii)

The active compounds were formulated in 50:50 acetone:water and 100 ppm Kinetic™ surfactant.

Cotton plants at the cotyledon stage (one plant per pot) were infested by placing a heavily infested leaf from the main colony on top of each cotyledon. The aphids were allowed to transfer to the host plant overnight, and the leaf used to transfer the aphids was removed. The cotyledons were dipped in the test solution and allowed to dry. After 5 days, mortality counts were made.

In this test, compound I.3-1, I.3-3, I.3-4, I.3-5, I.3-6, I.3-7, I.3-8, I.3-9, I.3-10, I.3-11, I.3-12, I.3-13, I.3-14, I.3-15, I.3-16, I.3-17, I.3-18, I.3-19, I.3-20, I.3-21, I.3-22, I.3-23, I.3-24, I.3-25, I.3-26, I.3-27, I.3-28, I.3-29, I.3-30, I.3-32, I.3-33, I.3-34, I.3-35, I.3-36, I.3-38, I.3-39, I.3-40, I.3-41, I.3-42, I.3-43, I.3-44, I.3-51, I.3-52, I.3-53, I.3-54, I.4-1, I.4-2, I.4-3, I.4-4, I.4-5, I.4-6, I.4-7, I.4-8, I.4-9, I.4-10, I.4-11, I.4-12, I.4-13 and I.4-16 at 300 ppm showed over 50% mortality.

7. Activity Against Southern Armyworm (Spodoptera eridania), 2nd Instar Larvae

The active compounds were formulated for testing the activity against insects and arachnids as a 10.000 ppm solution in a mixture of 35% acetone and water, which was diluted with water, if needed.

A Sieva lima bean leaf was dipped in the test solution and allowed to dry. The leaf was then placed in a petri dish containing a filter paper on the bottom and ten 2nd instar caterpillars. At 5 days, observations are made of mortality and reduced feeding.

In this test, compounds I.1-1, I.1-3, I.1-7, I.1-9, I.1-10, I.1-11, I.1-12, I.1-13, I.1-14, I.1-15, I.1-16, I.1-19, I.1-21, I.1-24, I.1-27, I.1-28, I.1-30, I.1-31, I.1-32, I.1-34, I.1-35, I.1-36, I.1-38, I.1-39, I.1-40, I.1-41, I.1-42, I.1-43, I.1-44, I.1-45, I.1-46, I.1-47, I.1-49, I.1-53, I.1-54, I.1-57, I.1-61, I.1-63, I.1-66, I.1-69, I.2-1, I.2-2, I.2-3, I.2-4, I.2-5, I.2-6, I.2-8, I.2-9, I.3-3, I.3-4, I.3-5, I.3-6, I.3-7, I.3-8, I.3-9, I.3-10, I.3-11, I.3-12, I.3-13, I.3-14, I.3-15, I.3-16, I.3-17, I.3-18, I.3-19, I.3-20, I.3-21, I.3-22, I.3-23, I.3-24, I.3-25, I.3-26, I.3-27, I.3-28, I.3-29, I.3-30, I.3-32, I.3-33, I.3-34, I.3-35, I.3-37, I.3-38, I.3-39, I.3-40, I.3-41, I.3-42, I.3-43, I.3-44, I.3-51, I.3-52, I.3-53, I.3-54, I.4-1, I.4-2, I.4-3, I.4-4, I.4-5, I.4-6, I.4-7, I.4-8, I.4-9, I.4-11, I.4-12, I.4-13, I.4-16, I.4-22 and I.4-23 at 300 ppm showed over 75% mortality.

8. Activity Against Silverleaf Whitefly (bemisia argentifolii)

The active compounds were formulated in 50:50 acetone:water and 100 ppm Kinetic™ surfactant.

Selected cotton plants were grown to the cotyledon state (one plant per pot). The cotyledons were dipped into the test solution to provide complete coverage of the foliage and placed in a well-vented area to dry. Each pot with treated seedling was placed in a plastic cup and 10 to 12 whitefly adults (approximately 3-5 day old) were introduced. The insects were collected using an aspirator and an 0.6 cm, non-toxic Tygon™ tubing (R-3603) connected to a barrier pipette tip. The tip, containing the collected insects, was then gently inserted into the soil containing the treated plant, allowing insects to crawl out of the tip to reach the foliage for feeding. The cups were covered with a reusable screened lid (150 micron mesh polyester screen PeCap from Tetko Inc). Test plants were maintained in the holding room at about 25° C. and 20-40% relative humidity for 3 days avoiding direct exposure to the fluorescent light (24 hour photoperiod) to prevent trapping of heat inside the cup. Mortality was assessed 3 days after treatment of the plants.

In this test, compound I.3-1, I.3-3, I.3-4, I.3-5, I.3-6, I.3-8, I.3-9, I.3-10, I.3-11, I.3-12, I.3-13, I.3-14, I.3-15, I.3-16, I.3-17, I.3-19, I.3-20, I.3-22, I.3-23, I.3-25, I.3-26, I.3-27, I.3-28, I.3-30, I.4-1, I.4-2 and I.4-3 at 300 ppm showed over 90% mortality.

9. Activity Against Diamond Back Moth (plutella xylostella)

The active compounds were formulated in 50:50 acetone:water and 0.1% (vol/vol) Alkamuls EL 620 surfactant. A 6 cm leaf disk of cabbage leaves was dipped in the test solution for 3 seconds and allowed to air dry in a Petri plate lined with moist filter paper. The leaf disk was inoculated with 10 third instar larvae and kept at 25-27° C. and 50-60% humidity for 3 days. Mortality was assessed after 72 h of treatment.

In this test, compounds I.1-1, I.1-7, I.1-9, I.1-15, I.1-19, I.1-21, I.1-24, I.1-27, I.1-28, I.1-29, I.1-31, I.1-32, I.1-45, I.1-47, I.1-61, I.1-63, I.3-5, I.3-6, I.3-7, I.3-8, I.3-9, I.3-10, I.3-11, I.3-12, I.3-13, I.3-14, I.3-15, I.3-16, I.3-17, I.3-18, I.3-19, I.3-20, I.3-21, I.3-22, I.3-23, I.3-24, I.3-25, I.3-26, I.3-27, I.3-28, I.3-29, I.3-30, I.3-31, I.3-32, I.3-33, I.3-34, I.3-35, I.3-36, I.3-37, I.3-38, I.3-39, I.3-40, I.3-41, I.3-42, I.3-43, I.3-44, I.3-45, I.3-46, I.3-47, I.3-48, I.3-49, I.3-51, I.3-52, I.3-53, I.3-54, I.3-55, I.3-56, I.3-57, I.3-58, I.3-59, I.3-60, I.3-61, I.3-62, I.3-63, I.4-1, I.4-2, I.4-3, I.4-4, I.4-5, I.4-6, I.4-7, I.4-8, I.4-9, I.4-10, I.4-11, I.4-12, I.4-13, I.4-16, I.4-17, I.4-18, I.4-19, and I.4-22 at 300 ppm showed over 75% mortality.

10. Activity Against Argentine Ant (Linepithema humile), Harvester Ant (Pogonomyrmex californicus), Acrobat Ant (Crematogaster Spp.), Carpenter Ant (Camponotus floridanus), Fire Ant (Solenopsis invicta), House Fly (Musca domestica), Stable Fly (Stomoxys calcitrans), Flesh Fly (Sarcophaga Sp.), Yellowfever Mosquito (Aedes aegyptii), House Mosquito (Culex quinquefasciatus), Malaria Mosquito (Anopheles albimanus), German Cockroach (Blattella germanica), Cat Flea (Ctenocephalides felis), and Brown Dog Tick (Rhipicephalus sanguineus) Via Glass Contact

Glass vials were treated with 0.5 ml of a solution of active ingredient in acetone and allowed to dry. Insects or ticks were placed into each vial together with some food and moisture supply. The vials were kept at 22° C. and were observed for treatment effects at various time intervals.

In this test, compounds I.3-4, 1.3-5 and I.3-6 at 10 ppm showed over 70% mortality of yellowfever mosquito.

11. Activity Against Yellowfever Mosquito (Aedes aegyptii), House Mosquito (Culex quinquefasciatus) and Malaria Mosquito (Anopheles albimanus) Larvae Via Water Treatment

Well plates were used as test arenas. The active ingredient was dissolved in acetone and diluted with water to obtain the concentrations needed. The final solutions containing appr. 1% acetone were placed into each well. Approximately 10 mosquito larvae (4th-instars) in 1 ml water were added to each well. Larvae were fed one drop of liver powder each day. The dishes were covered and maintained at 22° C. Mortality was recorded daily and dead larvae and live or dead pupae were removed daily. At the end of the test remaining live larvae were recorded and percent mortality was calculated.

In this test, compounds I.1-37, I.1-38, I.1-49, I.1-69, I.3-4, I.3-5, I.3-6 and I.3-7 at 10 ppm showed over 70% mortality of yellowfever mosquito.

12. Activity Against Root-Knot Nematode (Meloidogyne incognita):

Test compounds are prepared and formulated into aqueous formulations using acetone. Tomato plants (var. Bonny Best) are grown in the greenhouse in plastic tubs (4 to 6 plants per tub). The plants and soil (a 50:50 mixture of sand and “New Egypt” sandy loam) are infested with M. incognita J2 (to establish the “in-house” colony, M. incognita J2 were initially acquired from Auburn University). The plants are kept pruned and are used on an “as needed” basis. The tomato plants are kept in the cylinder containing hydroponic solution and aerated until the nematodes are no longer present in the solution (usually about 60 days). The cultures are checked daily by eluting a small volume (approximately 20 ml) from the bottom of a funnel attached to the cylinder into a small crystallizing dish and observed using a binocular dissecting scope. If needed for testing, the nematodes are cleaned and concentrated by pouring the culture solution through a sieve for cleaning and a sieve for concentrating. The nematodes are then resuspended in water to a concentration of approximately 20 to 50 nematodes per 50 μl. These are counted by putting 25 μl of the nematode solution into a well of an unused well of an assay plate. The total is then multiplied by 2 for a final total of nematodes per 50 μl of solution. To microtiter plates containing about 1.0 mg of compound, 80:20 acetone is added to each well and the solution is mixed to obtain the desired compound concentration. The nematode solution is added to each plate. The plates are then sealed and they are placed in an incubator at 27° C. and 50% (+/−2%) relative humidity. After 72 hours, the population mortality is read, whereby immobility of nematodes is regarded as mortality. 

1. A compound of formula I having the following structure,

wherein, R¹ is hydrogen; or C₁-C₁₀-alkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, or C₃-C₈-cycloalkyl, each of which is unsubstituted or substituted with 1 to 5 groups independently selected from halogen, cyano, nitro, hydroxy, C₁-C₁₀-alkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₂-C₁₀-alkoxycarbonyl, C₁-C₁₀-alkylamino, di(C₁-C₁₀-alkyl)amino and C₃-C₈-cycloalkylamino; or C₁-C₁₀-alkylcarbonyl, C₁-C₁₀-alkoxycarbonyl C₁-C₁₀-alkylaminocarbonyl, di(C₁-C₁₀-alkyl)aminocarbonyl; A is a group selected from A¹ and A²

wherein, # denotes the binding site, and m is 2; n is 0 or 1; R² and R³ each independently are R⁶, —C(=G)R⁷, —C(═NOR⁷)R⁷, —C(═NNR⁷ ₂)R⁷, —C(=G)OR⁷, —C(=G)NR⁷ ₂, —OC(=G)R⁷, —OC(=G)OR⁷, —NR⁷C(=G)R⁷, —N[C(=G)R⁷]2, —NR⁷C(=G)OR⁷, —C(=G)NR⁷—NR⁷ ₂, —C(=G)NR⁷—NR⁷[C(=G)R⁷], —NR⁷—C(=G)NR⁷ ₂, —NR⁷—NR⁷C(=G)R⁷, —NR⁷—N[C(=G)R⁷]₂, —N[(C=G)R⁷]—NR⁷ ₂, —NR⁷—NR⁷[(C=G)GR⁷], —NR⁷[(C=G)NR⁷ ₂, —NR⁷[C═NR⁷]R⁷, —NR⁷(C═NR⁷)NR⁷ ₂, —O—NR⁷ ₂, —O—NR⁷(C=G)R⁷, —SO₂NR⁷ ₂, —NR⁷SO₂R⁷, —SO₂OR⁷, —OSO2R⁷, —OR⁷, —NR⁷ ₂, —SR⁷, —SiR⁷ ₃, —PR⁷ ₂, —P(=G)R⁷, —SOR⁷, —SO₂R⁷, —PG₂R⁷ ₂, or —PG₃R⁷ ₂; or R² and R³ together with the sulfur atom to which they are attached form a saturated, partially unsaturated or unsaturated 3- to 8-membered ring which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, which ring can be fused with one or two saturated, partially unsaturated or unsaturated 5- to 6-membered rings which may contain 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, wherein all of the above rings are unsubstituted or substituted by any combination of 1 to 6 groups R⁸; G is oxygen or sulfur; R⁶ is C₁-C₂₀-alkyl, C₂-C₂₀-alkenyl, C₂-C₂₀-alkynyl, C₃-C₈-cycloalkyl, C₃-C₈-cycloalkenyl, C₃-C₈-cycloalkynyl, phenyl, naphthyl, biphenyl, or a saturated, partially unsaturated or unsaturated 3- to 8-membered ring system which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, wherein all of these groups are unsubstituted or substituted by any combination of 1 to 6 groups R⁸; R⁷ is hydrogen or R⁶; R⁸ is R⁹; or two groups R⁸ together with the atoms to which they are attached form a saturated, partially unsaturated or unsaturated 3- to 8-membered ring system which may contain 1 to 4 heteroatoms/heterogroups selected from oxygen, nitrogen, sulfur, SO and SO₂, and which ring system is unsubstituted or substituted with any combination of 1 to 6 groups R⁹; R⁹ is R¹⁰, R¹¹, —C(=G)R¹⁰, —C(═NOR¹⁰)R¹⁰, —C(═NNR¹⁰ ₂)R¹⁰, —C(=G)OR¹⁰, —C(=G)NR¹⁰ ₂, —OC(=G)R¹⁰, —OC(=G)R¹⁰, —NR¹⁰C(=G)R¹⁰, —N[C(=G)R¹⁰]2, —NR¹⁰C(=G)OR¹⁰, —C(=G)NR¹⁰—NR¹⁰ ₂, —C(=G)NR¹⁰—NR¹⁰[C(=G)R¹⁰], —NR¹⁰—C(=G)NR¹⁰ ₂, —NR¹⁰—NR¹⁰C(=G)R¹⁰, —NR¹⁰—N[C(=G)R¹⁰]₂, —N[(C=G)R¹⁰]—NR¹⁰ ₂, —NR¹⁰—NR¹⁰[(C=G)GR¹⁰], NR¹⁰[(C=G)NR¹⁰ ₂, —NR¹⁰[C═NR¹⁰]R¹⁰, —NR¹⁰(C═NR¹⁰)NR¹⁰ ₂, —O—NR¹⁰ ₂, —O—NR¹⁰(C=G)R¹⁰, —SO₂NR¹⁰ ₂, —NR¹⁰SO₂R¹⁰, —SO₂OR¹⁰, —OSO2R¹⁰, —OR¹⁰, —NR¹⁰ ₂, —SR¹⁰, —SiR¹⁰ ₃, —PR¹⁰ ₂, —P(=G)R¹⁰, —SOR¹⁰, —SO₂R¹⁰, —PG₂R¹⁰ ₂, —PG₃R¹⁰ ₂ or two groups R⁹ together are (=G), (═N—R¹⁰), (═CR¹⁰ ₂), (═CHR¹⁰, or (═CH₂); R¹⁰ is C₁-C₁₀-alkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, C₃-C₈-cycloalkyl, C₄-C₈-cycloalkenyl, C₃-C₈-cycloalkyl-C₁-C₄-alkyl, C₄-C₈-cycloalkenyl-C₁-C₄-alkyl, C₃-C₈-cycloalkyl-C₂-C₄-alkenyl, C₄-C₈-cycloalkenyl-C₂-C₄-alkenyl, C₁-C₁₀-alkyl-C₃-C₈-cycloalkyl, C₂-C₁₀-alkenyl-C₃-C₈-cycloalkyl, C₂-C₁₀-alkynyl-C₃-C₈-cycloalkyl, C₁-C₁₀-alkyl-C₄-C₈-cycloalkenyl, C₂-C₁₀-alkenyl-C₄-C₈-cycloalkenyl, C₂-C₁₀-alkynyl-C₄-C₈-cycloalkenyl, a saturated, partially unsaturated or unsaturated 3- to 8-membered ring system which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, wherein the above groups are unsubstituted or substituted with any combination of from 1 to 6 groups R¹¹; R¹¹ is halogen, cyano, nitro, hydroxy, mercapto, amino, formyl, C₁-C₁₀-alkylcarbonyl, C₁-C₁₀-alkoxy, C₂-C₁₀-alkenyloxy, C₂-C₁₀-alkynyloxy, C₁-C₁₀-haloalkoxy, C₃-C₁₀-haloalkenyloxy, C₃-C₁₀-haloalkynyloxy, C₃-C₈-cycloalkoxy, C₄-C₈-cycloalkenyloxy, C₃-C₈-halocycloalkoxy, C₄-C₈-halocycloalkenyloxy, C₃-C₈-cycloalkyl-C₁-C₄-alkoxy, C₄-C₈-cycloalkenyl-C₁-C₄-alkoxy, C₃-C₈-cycloalkyl-C₂-C₄-alkenyloxy, C₄-C₈-cycloalkenyl-C₂-C₄-alkenyloxy, C₁-C₁₀-alkyl-C₃-C₈-cycloalkoxy, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkoxy, C₁-C₁₀-alkynyl-C₃-C₈-cycloalkoxy, C₁-C₁₀-alkyl-C₃-C₈-cycloalkenyloxy, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkenyloxy, C₁-C₄ alkoxy-C₁-C₁₀-alkoxy, C₁-C₄-alkoxy-C₂-C₁₀-alkenyloxy, mono- or di(C₁-C₁₀-alkyl)carbamoyl, mono- or di(C₁-C₁₀-haloalkyl)carbamoyl, mono- or di(C₃-C₈-cycloalkyl)carbamoyl, C₁-C₁₀-alkoxycarbonyl, C₃-C₈-cycloalkoxycarbonyl, C₁-C₁₀-alkylcarbonyloxy, C₃-C₈-cyclo alkylcarbonyloxy, C₁-C₁₀-haloalkoxycarbonyl, C₁-C₁₀-haloalkylcarbonyloxy, C₁-C₁₀-alkanamido, C₁-C₁₀-haloalkanamido, C₂-C₁₀-alkenamido, C₃-C₈-cycloalkanamido, C₃-C₈-cycloalkyl-C₁-C₄-alkanamido, C₂-C₁₀-alkenylthio, C₂-C₁₀-alkynylthio, C₂-C₁₀-haloalkenylthio, C₂-C₁₀-haloalkynylthio, C₃-C₈-cycloalkylthio, C₃-C₈-cycloalkenylthio, C₃-C₈-halocycloalkylthio, C₃-C₈-halocycloalkenylthio, C₃-C₈-cycloalkyl-C₁-C₄-alkylthio, C₄-C₈-cycloalkenyl-C₁-C₄-alkylthio, C₃-C₈-cycloalkyl-C₂-C₄-alkenylthio, C₄-C₈-cycloalkenyl-C₂-C₄-alkenylthio, C₁-C₁₀-alkyl-C₃-C₈-cycloalkylthio, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkylthio, C₁-C₁₀-alkynyl-C₃-C₈-cycloalkylthio, C₁-C₁₀-alkyl-C₃-C₈-cycloalkenylthio, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkenylthio, C₁-C₁₀-alkylsulfinyl, C₂-C₁₀-alkenylsulfinyl, C₂-C₁₀-alkynylsulfinyl, C₁-C₁₀-haloalkylsulfinyl, C₂-C₁₀-haloalkenylsulfinyl, C₂-C₁₀-haloalkynylsulfinyl, C₃-C₈-cycloalkylsulfinyl, C₃-C₈-cycloalkenylsulfinyl, C₃-C₈-halocycloalkylsulfinyl, C₃-C₈-halocycloalkenylsulfinyl, C₃-C₈-cycloalkyl-C₁-C₄-alkylsulfinyl, C₄-C₈-cycloalkenyl-C₁-C₄-alkylsulfinyl, C₃-C₈-cycloalkyl-C₂-C₄-alkenylsulfinyl, C₄-C₈-cycloalkenyl-C₂-C₄-alkenylsulfinyl, C₁-C₁₀-alkyl-C₃-C₈-cycloalkylsulfinyl, alkenyl-C₃-C₈-cycloalkylsulfinyl, C₁-C₁₀-alkynyl-C₃-C₈-cycloalkylsulfinyl, C₁-C₁₀-alkyl-C₃-C₈-cycloalkenylsulfinyl, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkenylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₂-C₁₀-alkenylsulfonyl, C₂-C₁₀-alkynylsulfonyl, C₁-C₁₀-haloalkylsulfonyl, C₂-C₁₀-haloalkenylsulfonyl, C₂-C₁₀-haloalkynylsulfonyl, C₃-C₈-cycloalkylsulfonyl, C₃-C₈-cycloalkenylsulfonyl, C₃-C₈-halocycloalkylsulfonyl, C₃-C₈-halocycloalkenylsulfonyl, C₃-C₈-cycloalkyl-C₁-C₄-alkylsulfonyl, C₄-C₈-cycloalkenyl-C₁-C₄-alkylsulfonyl, C₃-C₈-cycloalkyl-C₂-C₄-alkenylsulfonyl, C₄-C₈-cycloalkenyl-C₂-C₄-alkenylsulfonyl, C₁-C₁₀-alkyl-C₃-C₈-cycloalkylsulfonyl, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkylsulfonyl, C₁-C₁₀-alkynyl-C₃-C₈-cycloalkylsulfonyl, C₁-C₁₀-alkyl-C₃-C₈-cycloalkenylsulfonyl, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkenylsulfonyl, di(C₁-C₁₀-alkyl)amino, C₁-C₁₀-alkylamino, C₂-C₁₀-alkenylamino, C₂-C₁₀-alkynylamino, C₁-C₁₀-alkyl-C₂-C₁₀-alkenylamino, C₁-C₁₀-alkyl-C₂-C₁₀-alkynylamino, C₁-C₁₀-haloalkylamino, C₂-C₁₀-haloalkenylamino, C₂-C₁₀-haloalkynylamino, C₃-C₈-cycloalkylamino, C₃-C₈-cycloalkenylamino, C₃-C₈-halocycloalkylamino, C₃-C₈-halocycloalkenylamino, C₃-C₈-cycloalkyl-C₁-C₄-alkylamino, C₄-C₈-cycloalkenyl-C₁-C₄-alkylamino, C₃-C₈-cycloalkyl-C₂-C₄-alkenylamino, C₄-C₈-cycloalkenyl-C₂-C₄-alkenylamino, C₁-C₁₀-alkyl-C₃-C₈-cycloalkylamino, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkylamino, C₁-C₁₀-alkynyl-C₃-C₈-cycloalkylamino, C₁-C₁₀-alkyl-C₃-C₈-cycloalkenylamino, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkenylamino, tri(C₁-C₁₀-alkyl)silyl, aryl, aryloxy, arylthio, arylamino, aryl-C₁-C₄-alkoxy, aryl-C₃-C₄-alkenyloxy, aryl-C₁-C₄-alkylthio, aryl-C₂-C₄-alkenylthio, aryl-C₁-C₄-alkylamino, aryl-C₃-C₄-alkenylamino, aryl-di(C₁-C₄-alkyl)silyl, triarylsilyl, wherein aryl is phenyl, naphthyl or biphenyl, or a saturated, partially unsaturated or unsaturated 3- to 8-membered ring system which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, wherein said aryl and heteroatom cyclic ringsystems are unsubstituted or substituted with any combination of from 1 to 6 groups selected from halogen, cyano, nitro, amino, hydroxy, mercapto, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₃-C₈-cycloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkylthio, C₁-C₄-haloalkylthio, di(C₁-C₄-alkyl)amino, C₁-C₄-alkylamino, C₁-C₄-haloalkylamino, formyl and C₁-C₄-alkylcarbonyl; R⁴ is NR¹²R¹³; R¹² and R¹³ are each independently hydrogen; or C₁-C₂₀-alkyl, C₂-C₂₀-alkenyl or C₂-C₂₀-alkynyl, each of which is unsubstituted or substituted with any combination of 1 to 6 groups selected from C₁-C₄-alkoxy, C₁-C₄-alkylthio, cyano, nitro, formyl, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxycarbonyl, C₁-C₄-alkylaminocarbonyl, di(C₁-C₄-alkyl)aminocarbonyl, C₁-C₄-alkylsulfinyl, C₁-C₄-alkylsulfonyl, C₃-C₈-cycloalkyl, and phenyl, wherein phenyl itself is unsubstituted or substituted by 1 to 4 substituents selected from halogen, C₁-C₄-alkyl, C₁-C₄-alkoxy, C₁-C₄-fluoroalkyl, C₁-C₄-alkyloxycarbonyl, trifluoromethylsulfonyl, formyl, nitro and cyano; or C₁-C₂₀-haloalkyl, C₂-C₂₀-haloalkenyl, C₂-C₂₀-haloalkynyl, C₅-C₁₀-cycloalkenyl, or a saturated or partially unsaturated or unsaturated 3- to 8-membered ring system which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, or phenyl or naphthyl, wherein this ring system and phenyl or naphthyl themselves are unsubstituted or substituted by 1 to 4 substituents selected from halogen, C₁-C₄-alkyl, C₁-C₄-alkoxy, C₁-C₄-fluoroalkyl, C₁-C₄-alkyloxycarbonyl, trifluoromethylsulfonyl, formyl, nitro and cyano; or R¹² and R¹³ together with the nitrogen atom to which they are attached form a saturated or partially unsaturated 5- to 8-membered heterocycle which besides the one nitrogen atom contains 0 to 2 further heteroatoms selected from oxygen, nitrogen, sulfur, and may contain 1 or 2 carbonyl groups or thiocarbonyl groups and which is unsubstituted or substituted by from 1 to 4 groups selected from C₁-C₄-alkyl, C₁-C₄-alkoxy and C₁-C₄-haloalkyl; R⁵ is hydrogen; or C₁-C₂₀-alkyl, C₂-C₂₀-alkenyl, C₂-C₂₀-alkynyl, C₁-C₄-alkylcarbonyl, C₁-C₄-alkylaminocarbonyl, C₁-C₄-alkoxycarbonyl, each of which is unsubstituted or substituted by from 1 to 6 groups selected from C₁-C₄-alkoxy, C₁-C₄-alkylthio, cyano, nitro, formyl, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxycarbonyl, C₁-C₄-alkylaminocarbonyl, di(C₁-C₄-alkyl)aminocarbonyl, C₁-C₄-alkylsulfinyl, C₁-C₄-alkylsulfonyl, C₃-C₈-cycloalkyl, and phenyl, wherein phenyl itself is unsubstituted or substituted by 1 to 4 substituents selected from halogen, C₁-C₄-alkyl, C₁-C₄-alkoxy, C₁-C₄-fluoroalkyl, C₁-C₄-alkyloxycarbonyl, trifluoromethylsulfonyl, formyl, nitro and cyano; or C₁-C₂₀-haloalkenyl, C₂-C₂₀-haloalkynyl, C₅-C₁₀-cycloalkenyl, or a saturated or partially unsaturated or unsaturated 3- to 8-membered ring system which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, or phenyl or naphthyl, wherein this ring system and phenyl or naphthyl themselves are unsubstituted or substituted by 1 to 4 substituents selected from halogen, C₁-C₄-alkyl, C₁-C₄-alkoxy, C₁-C₄-fluoroalkyl, C₁-C₄-alkyloxycarbonyl, trifluoromethylsulfonyl, formyl, nitro and cyano; Q¹ and Q² each independently are hydrogen, halogen, cyano, SCN, nitro, hydroxy, C₁-C₁₀-alkyl, C₁-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-haloalkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-haloalkylsulfonyl, C₁-C₁₀-alkylsulfonyloxy, C₁-C₁₀-haloalkylsulfonyloxy, C₁-C₁₀-alkylamino, di(C₁-C₁₀-alkyl)amino, C₃-C₈-cyclalkylamino, alkylcarbonyl, C₁-C₁₀-alkoxycarbonyl, C₁-C₁₀-alkylaminocarbonyl, di(C₁-C₁₀-alkyl)aminocarbonyl, or tri(C₁-C₁₀)-alkylsilyl, or Q¹ and Q² are each independently phenyl, benzyl or phenoxy, wherein each ring is unsubstituted or substituted with any combination of from 1 to 3 substituents independently selected from the group halogen, cyano, nitro, C₁-C₁₀-alkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-alkylamino, di(C₁-C₁₀-alkyl)amino, C₃-C₈-cycloalkylamino, C₁-C₁₀-alkyl-C₃-C₈-cycloalkylamino, C₁-C₁₀-alkylcarbonyl, C₁-C₁₀-alkoxycarbonyl, C₁-C₁₀-alkylaminocarbonyl, di(C₁-C₁₀-alkyl)aminocarbonyl and tri(C₁-C₁₀)-alkylsilyl; Q³ is halogen; or C₁-C₁₀-alkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₁₀-alkyl-C₃-C₈-cycloalkyl, C₁-C₁₀-haloalkyl-C₃-C₈-cycloalkyl, each unsubstituted or independently substituted with 1 to 2 groups selected from cyano, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-haloalkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-haloalkylsulfonyl, and C₁-C₁₀-alkoxycarbonyl; or Q³ is OR¹⁴, S(O)_(q)R¹⁴, NR¹⁵R¹⁶, OS(O)₂R⁷, NR¹⁶S(O)₂R¹⁷, C(S)NH₂, C(R¹⁸)═NOR¹⁸, C₃-C₈cycloalkyl-C₁-C₄, C₁-C₁₀-alkylaminothiocarbonyl, or di(C₁-C₁₀-alkyl)aminothiocarbonyl; R¹⁴ is C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₃-C₈-cycloalkyl-C₁-C₄-alkyl, C₁-C₄-alkyl-C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl-C₁-C₄-alkyl, C₁-C₄-haloalkyl-C₃-C₈-cycloalkyl, or C₁-C₁₀-haloalkylcarbonyl, each unsubstituted or substituted with one R¹⁹; R¹⁵ is C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₄-alkyl-C₃-C₈-cycloalkyl, C₁-C₄-haloalkyl-C₃-C₈-cycloalkyl, or C₁-C₁₀-haloalkylcarbonyl, each unsubstituted or substituted with one R¹⁹; R¹⁶ is hydrogen; or C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₄-alkyl-C₃-C₈-cycloalkyl, or C₁-C₄-haloalkyl-C₃-C₈-cycloalkyl, each unsubstituted or substituted with one R¹⁹; R¹⁷ is C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₄-alkyl-C₃-C₈-cycloalkyl, or C₁-C₄-haloalkyl-C₃-C₈-cycloalkyl, each unsubstituted or substituted with one R¹⁹; R¹⁹ is cyano, nitro, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-haloalkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-haloalkylsulfonyl, C₁-C₁₀-alkoxycarbonyl, C₁-C₁₀-alkylamino, or di(C₁-C₁₀-alkyl)amino; or R¹⁹ is phenyl or a heteroaromatic 5- or 6-membered ring which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, the phenyl radical and the heteroaromatic ring being unsubstituted or substituted with any combination of from 1 to 3 groups selected from halogen, cyano, nitro, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-alkylamino, di(C₁-C₁₀-alkyl)amino, C₃-C₈-cycloalkylamino, C₁-C₁₀-alkyl-C₃-C₈-cycloalkylamino, C₁-C₁₀-alkylcarbonyl, C₁-C₁₀-alkoxycarbonyl, C₁-C₁₀-alkylaminocarbonyl, di(C₁-C₁₀-alkyl)aminocarbonyl and tri(C₁-C₁₀)-alkylsilyl; R¹⁸ in each instance is hydrogen, C₁-C₁₀-alkyl, or C₁-C₁₀-haloalkyl; q is 0, 1 or 2; Q⁴ is halogen, cyano, nitro, hydroxy, COOH, C(O)NH₂, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-haloalkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-haloalkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-haloalkylsulfonyl, C₁-C₁₀-alkylamino, di(C₁-C₁₀-alkyl)amino, C₃-C₈-cycloalkylamino, C₁-C₁₀-alkylcarbonyl, C₁-C₁₀-alkoxycarbonyl C₁-C₁₀-alkylaminocarbonyl, di(C₁-C₁₀-alkyl)aminocarbonyl or tri(C₁-C₁₀)-alkylsilyl; or Q⁴ is phenyl, benzyl, benzyloxy, phenoxy, a 5- or 6-membered heteroaromatic ring which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur or an aromatic 8-, 9- or 10-membered fused heterobicyclic ring system which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, wherein each of the above ring systems is unsubstituted or substituted with any combination of from 1 to 3 groups selected from halogen, cyano, nitro, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-alkylamino, di(C₁-C₁₀-alkyl)amino, C₃-C₈-cycloalkylamino, C₁-C₁₀-alkyl-C₃-C₈-cycloalkylamino, alkylcarbonyl, C₁-C₁₀-alkoxycarbonyl, C₁-C₁₀-alkylaminocarbonyl, di(C₁-C₁₀-alkyl)aminocarbonyl and tri(C₁-C₁₀)-alkylsilyl; X and Y are each independently oxygen or sulfur; V and V′ are each independently N or CQ²; W is N, CH or CQ⁴; and p is 0, 1, 2, 3, or 4; or the enantiomers or salts or N-oxides thereof.
 2. The compound of claim 1, wherein X and Y are oxygen.
 3. The compound of claim 2, wherein V and V′ are CH.
 4. The compound of claim 1, wherein V and V′ are CH.
 5. The compound of claim 4, wherein W is N; R¹ is hydrogen or C₁-C₄-alkyl; Q¹ is halogen, cyano, SCN, nitro, hydroxy, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₃-C₈-cycloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-alkylsulfonyloxy, C₁-C₁₀-alkylamino or di(C₁-C₁₀-alkyl)amino; Q² is halogen, cyano, SCN, nitro, hydroxy, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₃-C₈-cycloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-alkylsulfonyloxy, C₁-C₁₀-alkylamino or di(C₁-C₁₀-alkyl)amino; Q³ is halogen, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, each unsubstituted or independently substituted with 1 to 2 groups selected from cyano, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy or C₁-C₁₀-alkylthio, or Q³ is OR¹⁴, S(O)_(q)R¹⁴, NR¹⁵R¹⁶, OS(O)₂R¹⁷, C(S)NH₂, C(R¹⁸)═NOR¹⁸; wherein R¹⁴ is C₁-C₁₀-alkyl or C₃-C₈-cycloalkyl unsubstituted or substituted with 1 R¹⁹; and R¹⁵ is C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, each unsubstituted or substituted with one R¹⁹; and R¹⁶ is hydrogen, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, each unsubstituted or substituted with one R¹⁹; and R¹⁷ is C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, C₃-C₈-cycloalkyl, each unsubstituted or substituted with 1 R¹⁹; and R¹⁹ is cyano, nitro, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio; Q⁴ is halogen, cyano, nitro, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-haloalkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-haloalkylsulfonyl, or C₁-C₁₀-alkoxycarbonyl, and is in the ortho-position; and p is
 1. 6. The compound of claim 2, wherein W is N; R¹ is hydrogen or C₁-C₄-alkyl; Q¹ is halogen, cyano, SCN, nitro, hydroxy, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₃-C₈-cycloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-alkylsulfonyloxy, C₁-C₁₀-alkylamino or di(C₁-C₁₀-alkyl)amino; Q² is halogen, cyano, SCN, nitro, hydroxy, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₃-C₈-cycloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-alkylsulfonyloxy, C₁-C₁₀-alkylamino or di(C₁-C₁₀-alkyl)amino; Q³ is halogen, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, each unsubstituted or independently substituted with 1 to 2 groups selected from cyano, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy or C₁-C₁₀-alkylthio, or Q³ is OR¹⁴, S(O)_(q)R¹⁴, NR¹⁵R₁₆, OS(O)₂R¹⁷, C(S)NH₂, C(R¹⁸)═NOR¹⁸; wherein R¹⁴ is C₁-C₁₀-alkyl or C₃-C₈-cycloalkyl unsubstituted or substituted with 1 R¹⁹; and R¹⁵ is C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, each unsubstituted or substituted with one R¹⁹; and R¹⁶ is hydrogen, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, each unsubstituted or substituted with one R¹⁹; and R¹⁷ is C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, C₃-C₈-cycloalkyl, each unsubstituted or substituted with 1 R¹⁹; and R¹⁹ is cyano, nitro, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio; Q⁴ is halogen, cyano, nitro, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-haloalkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-haloalkylsulfonyl, or C₁-C₁₀-alkoxycarbonyl, and is in the ortho-position; and p is
 1. 7. The compound of claim 1, wherein W is N; R¹ is hydrogen or C₁-C₄-alkyl; Q¹ is halogen, cyano, SCN, nitro, hydroxy, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₃-C₈-cycloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-alkylsulfonyloxy, C₁-C₁₀-alkylamino or di(C₁-C₁₀-alkyl)amino; Q² is halogen, cyano, SCN, nitro, hydroxy, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₃-C₈-cycloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-alkylsulfonyloxy, C₁-C₁₀-alkylamino or di(C₁-C₁₀-alkylamino; Q³ is halogen, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, each unsubstituted or independently substituted with 1 to 2 groups selected from cyano, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy or C₁-C₁₀-alkylthio, or Q³ is OR¹⁴, S(O)_(q)R¹⁴, NR¹⁵R¹⁶, OS(O)₂R¹⁷, C(S)NH₂, C(R¹⁸)═NOR¹⁸; wherein R¹⁴ is C₁-C₁₀-alkyl or C₃-C₈-cycloalkyl unsubstituted or substituted with 1 R¹⁹; and R¹⁵ is C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, each unsubstituted or substituted with one R¹⁹; and R¹⁶ is hydrogen, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, each unsubstituted or substituted with one R¹⁹; and R¹⁷ is C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, C₃-C₈-cycloalkyl, each unsubstituted or substituted with 1 R¹⁹; and R¹⁹ is cyano, nitro, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio; Q⁴ is halogen, cyano, nitro, C₁-C₁₀-alkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-haloalkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-haloalkylsulfonyl, or C₁-C₁₀-alkoxycarbonyl, and is in the ortho-position; and p is
 1. 8. The compound of claim 7, wherein W is N; R¹ is hydrogen; Q¹ is hydrogen, halogen, cyano, C₁-C₄-alkyl or C₁-C₄-haloalkyl; Q² is halogen, cyano, C₁-C₄-alkyl or C₁-C₄-haloalkyl; Q³ is halogen, C₁-C₄-haloalkyl or C₁-C₄-haloalkoxy; Q⁴ is halogen or C₁-C₄-haloalkyl and is in the ortho-position; and p is
 1. 9. The compound of claim 4, wherein W is N; R¹ is hydrogen; Q¹ is hydrogen, halogen, cyano, C₁-C₄-alkyl or C₁-C₄-haloalkyl; Q² is halogen, cyano, C₁-C₄-alkyl or C₁-C₄-haloalkyl; Q³ is halogen, C₁-C₄-haloalkyl or C₁-C₄-haloalkoxy; Q⁴ is halogen or C₁-C₄-haloalkyl and is in the ortho-position; and p is
 1. 10. The compound of claim 2, wherein W is N; R¹ is hydrogen; Q¹ is hydrogen, halogen, cyano, C₁-C₄-alkyl or C₁-C₄-haloalkyl; Q² is halogen, cyano, C₁-C₄-alkyl or C₁-C₄-haloalkyl; Q³ is halogen, C₁-C₄-haloalkyl or C₁-C₄-haloalkoxy; Q⁴ is halogen or C₁-C₄-haloalkyl and is in the ortho-position; and p is
 1. 11. The compound of claim 1, wherein W is N; R¹ is hydrogen; Q¹ is hydrogen, halogen, cyano, C₁-C₄-alkyl or C₁-C₄-haloalkyl; Q² is halogen, cyano, C₁-C₄-alkyl or C₁-C₄-haloalkyl; Q³ is halogen, C₁-C₄-haloalkyl or C₁-C₄-haloalkoxy; Q⁴ is halogen or C₁-C₄-haloalkyl and is in the ortho-position; and p is
 1. 12. The compound of claim 11, wherein A is A¹; R² and R³ each independently is C₁-C₁₀-alkenyl, C₂-C₁₀-alkynyl, C₃-C₈-cycloalkyl, or phenyl, wherein these groups are unsubstituted or substituted by any combination of 1 to 6 groups selected from R¹¹, R¹¹ is halogen, cyano, nitro, hydroxy, mercapto, amino, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₃-C₈-cycloalkoxy, C₁-C₁₀-alkoxycarbonyl, C₁-C₁₀-alkylcarbonyloxy, C₁-C₁₀-alkanamido, C₁-C₁₀-alkylthio, C₁-C₁₀-alkylsulfonyl, di(C₁-C₁₀-alkyl)amino or C₁-C₁₀-alkylamino; or R² and R³ together with the sulfur atom to which they are attached form a unit SR²R³ of the following formula:

wherein r is 0 or 1; D is a direct bond, branched or straight C₁-C₄-alkylene, O, S(O)_(0,1,2) or NR^(j); R⁹ is as defined above; R^(j) is hydrogen, C₁-C₄-alkyl, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxycarbonyl, C₁-C₄-alkylaminocarbonyl, di(C₁-C₄-alkyl)aminocarbonyl, or C₁-C₄-alkylsulfonyl; and a and b are each independently 0, 1, 2, 3 or
 4. 13. The compound of claim 7, wherein A is A¹; R² and R³ each independently is C₁-C₁₀-alkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, C₃-C₈-cycloalkyl, or phenyl, wherein these groups are unsubstituted or substituted by any combination of 1 to 6 groups selected from R¹¹, R¹¹ is halogen, cyano, nitro, hydroxy, mercapto, amino, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₃-C₈-cycloalkoxy, C₁-C₁₀-alkoxycarbonyl, C₁-C₁₀-alkylcarbonyloxy, C₁-C₁₀-alkanamido, C₁-C₁₀-alkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-alkylsulfonyl, di(C₁-C₁₀-alkyl)amino or C₁-C₁₀-alkylamino; or R² and R³ together with the sulfur atom to which they are attached form a unit SR²R³ of the following formula:

wherein r is 0 or 1; D is a direct bond, branched or straight C₁-C₄-alkylene, O, S(O)_(0,1,2) or NR^(j); R⁹ is as defined above; R^(j) is hydrogen, C₁-C₄-alkyl, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxycarbonyl, C₁-C₄-alkylaminocarbonyl, di(C₁-C₄-alkyl)aminocarbonyl, or C₁-C₄-alkylsulfonyl; and a and b are each independently 0, 1, 2, 3 or
 4. 14. The compound of claim 4, wherein A is A¹; R² and R³ each independently is C₁-C₁₀-alkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, C₃-C₈-cycloalkyl, or phenyl, wherein these groups are unsubstituted or substituted by any combination of 1 to 6 groups selected from R¹¹, R¹¹ is halogen, cyano, nitro, hydroxy, mercapto, amino, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₃-C₈-cycloalkoxy, C₁-C₁₀-alkoxycarbonyl, C₁-C₁₀-alkylcarbonyloxy, C₁-C₁₀-alkanamido, C₁-C₁₀-alkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-alkylsulfonyl, di(C₁-C₁₀-alkyl)amino or C₁-C₁₀-alkylamino; or R² and R³ together with the sulfur atom to which they are attached form a unit SR²R³ of the following formula:

wherein r is 0 or 1; D is a direct bond, branched or straight C₁-C₄-alkylene, O, S(O)_(0,1,2) or NR^(j); R⁹ is as defined above; R^(j) is hydrogen, C₁-C₄-alkyl, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxycarbonyl, C₁-C₄-alkylaminocarbonyl, di(C₁-C₄-alkyl)aminocarbonyl, or C₁-C₄-alkylsulfonyl; and a and b are each independently 0, 1, 2, 3 or
 4. 15. The compound of claim 2, wherein A is A¹; R² and R³ each independently is C₁-C₁₀-alkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, C₃-C₈-cycloalkyl, or phenyl, wherein these groups are unsubstituted or substituted by any combination of 1 to 6 groups selected from R¹¹, R¹¹ is halogen, cyano, nitro, hydroxy, mercapto, amino, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₃-C₈-cycloalkoxy, C₁-C₁₀-alkoxycarbonyl, C₁-C₁₀-aIkylcarbonyloxy, C₁-C₁₀-alkanamido, C₁-C₁₀-alkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-alkylsulfonyl, di(C₁-C₁₀-alkyl)amino or C₁-C₁₀-alkylamino; or R² and R³ together with the sulfur atom to which they are attached form a unit SR²R³ of the following formula:

wherein r is 0 or 1; D is a direct bond, branched or straight C₁-C₄-alkylene, O, S(O)_(0,1,2) or NR^(j); R⁹ is as defined above; R^(j) is hydrogen, C₁-C₄-alkyl, C₁-C₄-alkylcarbonyl, C₁-C₄ alkoxycarbonyl, C₁-C₄-alkylaminocarbonyl, di(C₁-C₄-alkyl)aminocarbonyl, or C₁-C₄-alkylsulfonyl; and a and b are each independently 0, 1, 2, 3 or
 4. 16. The compound of claim 1, wherein A is A¹; R² and R³ each independently is C₁-C₁₀-alkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, C₃-C₈-cycloalkyl, or phenyl, wherein these groups are unsubstituted or substituted by any combination of 1 to 6 groups selected from R¹¹, R¹¹ is halogen, cyano, nitro, hydroxy, mercapto, amino, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₃-C₈-cycloalkoxy, C₁-C₁₀-alkoxycarbonyl, C₁-C₁₀-aIkylcarbonyloxy, C₁-C₁₀-alkanamido, C₁-C₁₀-alkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-alkylsulfonyl, di(C₁-C₁₀-alkyl)amino or C₁-C₁₀-alkylamino; or R² and R³ together with the sulfur atom to which they are attached form a unit SR²R³ of the following formula:

wherein r is 0 or 1; D is a direct bond, branched or straight C₁-C₄-alkylene, O, S(O)_(0,1,2) or NR³; R⁹ is as defined above; R^(j) is hydrogen, C₁-C₄-alkyl, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxycarbonyl, C₁-C₄-alkylaminocarbonyl, di(C₁-C₄-alkyl)aminocarbonyl, or C₁-C₄-alkylsulfonyl; and a and b are each independently 0, 1, 2, 3 or
 4. 17. The compound of claim 16, wherein A is A²; R⁴ is NR¹²R¹³ and R¹² and R¹³ are each independently hydrogen, C₁-C₂₀-alkyl, C₂-C₂₀-alkenyl or C₂-C₂₀-alkynyl, each of which is unsubstituted or substituted by from 1 to 3 CN, C₁-C₂₀-haloalkyl, or R¹² and R¹³ together with the nitrogen atom to which they are attached may also form a saturated or partially unsaturated 5- to 8-membered heterocycle which besides the one nitrogen atom contains 0 to 2 further heteroatoms selected from oxygen, nitrogen, sulfur, and may contain 1 or 2 carbonyl groups or thiocarbonyl groups and which is unsubstituted or substituted by from 1 to 4 groups selected from C₁-C₄-alkyl, C₁-C₄-alkoxy and C₁-C₄-haloalkyl; and R⁵ is hydrogen.
 18. The compound of claim 11, wherein A is A²; R⁴ is NR¹²R¹³ and R¹² and R¹³ are each independently hydrogen, C₁-C₂₀-alkyl, C₂-C₂₀-alkenyl or C₂-C₂₀-alkynyl, each of which is unsubstituted or substituted by from 1 to 3 CN, C₁-C₂₀-haloalkyl, or R¹² and R¹³ together with the nitrogen atom to which they are attached may also form a saturated or partially unsaturated 5- to 8-membered heterocycle which besides the one nitrogen atom contains 0 to 2 further heteroatoms selected from oxygen, nitrogen, sulfur, and may contain 1 or 2 carbonyl groups or thiocarbonyl groups and which is unsubstituted or substituted by from 1 to 4 groups selected from C₁-C₄-alkyl, C₁-C₄alkoxy and C₁-C₄-haloalkyl; and R⁵ is hydrogen.
 19. The compound of claim 7, wherein A is A²; R⁴ is NR¹²R¹³ and R¹² and R¹³ are each independently hydrogen, C₁-C₂₀-alkyl, C₂-C₂₀-alkenyl or C₂-C₂₀-alkynyl, each of which is unsubstituted or substituted by from 1 to 3 CN, C₁-C₂₀-haloalkyl, or R¹² and R¹³ together with the nitrogen atom to which they are attached may also form a saturated or partially unsaturated 5- to 8-membered heterocycle which besides the one nitrogen atom contains 0 to 2 further heteroatoms selected from oxygen, nitrogen, sulfur, and may contain 1 or 2 carbonyl groups or thiocarbonyl groups and which is unsubstituted or substituted by from 1 to 4 groups selected from C₁-C₄-alkyl, C₁-C₄-alkoxy and C₁-C₄-haloalkyl; and R⁵ is hydrogen.
 20. The compound of claim 4, wherein A is A²; R⁴ is NR¹², R¹³ and R¹² and R¹³ are each independently hydrogen, C₁-C₂₀-alkyl, C₂-C₂₀-alkenyl or C₂-C₂₀-alkynyl, each of which is unsubstituted or substituted by from 1 to 3 CN, C₁-C₂₀-haloalkyl, or R¹² and R¹³ together with the nitrogen atom to which they are attached may also form a saturated or partially unsaturated 5- to 8-membered heterocycle which besides the one nitrogen atom contains 0 to 2 further heteroatoms selected from oxygen, nitrogen, sulfur, and may contain 1 or 2 carbonyl groups or thiocarbonyl groups and which is unsubstituted or substituted by from 1 to 4 groups selected from C₁-C₄-alkyl, C₁-C₄-alkoxy and C₁-C₄-haloalkyl; and R⁵ is hydrogen.
 21. The compound of claim 2, wherein A is A²; R⁴ is NR¹²R¹³ and R¹² and R¹³ are each independently hydrogen, C₁-C₂₀-alkyl, C₂-C₂₀-alkenyl or C₂-C₂₀-alkynyl, each of which is unsubstituted or substituted by from 1 to 3 CN, C₁-C₂₀-haloalkyl, or R¹² and R¹³ together with the nitrogen atom to which they are attached may also form a saturated or partially unsaturated 5- to 8-membered heterocycle which besides the one nitrogen atom contains 0 to 2 further heteroatoms selected from oxygen, nitrogen, sulfur, and may contain 1 or 2 carbonyl groups or thiocarbonyl groups and which is unsubstituted or substituted by from 1 to 4 groups selected from C₁-C₄-alkyl, C₁-C₄-alkoxy and C₁-C₄-haloalkyl; and R⁵ is hydrogen.
 22. The compound of claim 1, wherein A is A²; R⁴ is NR¹²R¹³ and R¹² and R¹³ are each independently hydrogen, C₁-C₂₀-alkyl, C₂-C₂₀-alkenyl or C₂-C₂₀-alkynyl, each of which is unsubstituted or substituted by from 1 to 3 CN, C₁-C₂₀-haloalkyl, or R¹² and R¹³ together with the nitrogen atom to which they are attached may also form a saturated or partially unsaturated 5- to 8-membered heterocycle which besides the one nitrogen atom contains 0 to 2 further heteroatoms selected from oxygen, nitrogen, sulfur, and may contain 1 or 2 carbonyl groups or thiocarbonyl groups and which is unsubstituted or substituted by from 1 to 4 groups selected from C₁-C₄-alkyl, C₁-C₄-alkoxy and C₁-C₄-haloalkyl; and R⁵ is hydrogen.
 23. A process for the preparation of compounds of claim 2, said method comprising, contacting in the presence of a base an activated compound of the formula (II),

with a compound of the formula A¹-H or A²-H,

wherein the compound of claim 24 is prepared.
 24. A method for the control of insects, acarids or nematodes comprising, contacting said insect, acarid or nematode or their food supply, habitat, breeding ground or their locus with a pesticidally effective amount of one or more compounds of claim 1, wherein said insects, acarids or nematodes are controlled.
 25. A method of protecting growing plants from attack or infestation by insects, acarids or nematodes comprising, applying to the foliage of the plants, or to the soil or water in which said plants are growing a pesticidally effective amount of one or more compounds of claim 1, wherein said plants are protected.
 26. A method for treating an animal infected by parasites or controlling or protecting the animal against infestation or infection by parasites comprising, administering orally, topically or parenterally, or applying to said animal a parasiticidally effective amount of one or more compounds of claim 1, wherein said animal is treated or protected against said infestation or infection by parasites; or wherein said infestation or infection by parasites is controlled.
 27. A process for the preparation of a composition for treating, controlling or protecting animals against infestation or infection by parasites comprising, contacting one or more compounds of formula I,

wherein, R¹ is hydrogen; or C₁-C₁₀-alkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, or C₃-C₈-cycloalkyl, each of which is unsubstituted or substituted with 1 to 5 groups independently selected from halogen, cyano, nitro, hydroxy, C₁-C₁₀-alkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₂-C₁₀-alkoxycarbonyl, C₁-C₁₀-alkylamino, di(C₁-C₁₀-alkyl)amino and C₃-C₈-cycloalkylamino; or C₁-C₁₀-alkylcarbonyl, C₁-C₁₀-alkoxycarbonyl C₁-C₁₀-alkylaminocarbonyl, di(C₁-C₁₀-alkyl)aminocarbonyl; A is a group selected from A¹ and A²

wherein, # denotes the binding site, and m is 2; n is 0 or 1; R² and R³ each independently are R⁶; —C(=G)R⁷, —C(═NOR⁷)R⁷, —C(═NNR⁷ ₂)R⁷, —C(=G)OR⁷, —C(=G)NR⁷ ₂, —OC(=G)OR⁷, —OC(=G)OR⁷, —NR⁷C(=G)R⁷, —N[C(=G)R⁷]2, —NR⁷C(=G)OR⁷, —C(=G)NR⁷—NR⁷ ₂, —C(=G)NR⁷—NR⁷[C(=G)R⁷], —NR⁷—C(=G)NR⁷ ₂, —NR⁷—NR⁷C(=G)R⁷, —NR⁷—N[C(=G)R⁷]₂, —N[(C=G)R⁷]—NR⁷ ₂, —NR⁷—NR⁷—[(C=G)GR⁷], —NR⁷[(C=G)NR⁷ ₂, —NR⁷[C═NR⁷]R⁷, —NR⁷(C═NR⁷)NR⁷ ₂, —O—NR⁷ ₂, —O—NR⁷(C=G)R⁷, —SO₂NR⁷ ₂, —NR⁷SO₂R⁷, —SO₂OR⁷, —OSO2R⁷, —OR⁷, —NR⁷ ₂, —SR⁷, —SiR⁷ ₃, —PR⁷ ₂, —P(=G)R⁷, —SOR⁷, —SO₂R⁷, —PG₂R⁷ ₂, or —PG₃R⁷ ₂; or R² and R³ together with the sulfur atom to which they are attached form a saturated, partially unsaturated or unsaturated 3- to 8-membered ring which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, which ring can be fused with one or two saturated, partially unsaturated or unsaturated 5- to 6-membered rings which may contain 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, wherein all of the above rings are unsubstituted or substituted by any combination of 1 to 6 groups R⁸; G is oxygen or sulfur; R⁶ is C₁-C₂₀-alkyl, C₂-C₂₀-alkenyl, C₂-C₂₀-alkynyl, C₃-C₈-cycloalkyl, C₃-C₈-cycloalkenyl, C₃-C₈-cycloalkynyl, phenyl, naphthyl, biphenyl, or a saturated, partially unsaturated or unsaturated 3- to 8-membered ring system which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, wherein all of these groups are unsubstituted or substituted by any combination of 1 to 6 groups R⁸; R⁷ is hydrogen or R⁶; R⁸ is R⁹; or two groups R⁸ together with the atoms to which they are attached form a saturated, partially unsaturated or unsaturated 3- to 8-membered ring system which may contain 1 to 4 heteroatoms/heterogroups selected from oxygen, nitrogen, sulfur, SO and SO₂, and which ring system is unsubstituted or substituted with any combination of 1 to 6 groups R⁹; R⁹ is R¹⁰, R¹¹, —C(=G)R¹⁰, —C(═NOR¹⁰)R¹⁰, —C(═NNR¹⁰ ₂)R¹⁰, —C(=G)OR¹⁰, —C(=G)NR¹⁰ ₂, —OC(=G)R¹⁰, —OC(=G)OR¹⁰, —NR¹⁰C(=G)R¹⁰, —N[C(=G)R¹⁰]2, —NR¹⁰C(=G)OR¹⁰, —C(=G)NR¹⁰ ₂, —C(=G)NR¹⁰—NR¹⁰[C(=G)R¹⁰], —NR¹⁰—C(=G)NR¹⁰ ₂, —NR¹⁰—NR¹⁰C(=G)R¹⁰, —NR¹⁰—N[C(=G)R¹⁰]₂, —N[(C=G)R¹⁰]—NR¹⁰ ₂, —NR¹⁰—NR¹⁰[(C=G)GR¹⁰], —NR¹⁰[(C=G)NR¹⁰ ₂, —NR¹⁰[C═NR¹⁰]R¹⁰, —NR¹⁰(C═NR¹⁰)NR¹⁰ ₂, —O—NR¹⁰ ₂, —O—NR¹⁰(C=G)R¹⁰, —SO₂NR¹⁰ ₂, —NR¹⁰SO₂R¹⁰, —SO₂OR¹⁰, —OSO2R¹⁰, —OR¹⁰, —NR¹⁰ ₂, —SR¹⁰, SiR¹⁰ ₃, —PR¹⁰ ₂, —P(=G)R¹⁰, —SOR¹⁰, SO₂R¹⁰, —PG₂R¹⁰ ₂, —PG₃R¹⁰ ₂ or two groups R⁹ together are (=G), (═N—R¹⁰), (═CR¹⁰ ₂), (═CHR¹⁰), or (═CH₂); R¹⁰ is C₁-C₁₀-alkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, C₃-C₈-cycloalkyl, C₄-C₈-cycloalkenyl, C₃-C₈-cycloalkyl-C₁-C₄-alkyl, C₄-C₈-cycloalkenyl-C₁-C₄-alkyl, C₃-C₈-cycloalkyl-C₂-C₄-alkenyl, C₄-C₈-cycloalkenyl-C₂-C₄-alkenyl, C₁-C₁₀-alkyl-C₃-C₈-cycloalkyl, C₂-C₁₀-alkenyl-C₃-C₈-cycloalkyl, C₂-C₁₀-alkynyl-C₃-C₈-cycloalkyl, C₁-C₁₀-alkyl-C₄-C₈-cycloalkenyl, C₂-C₁₀-alkenyl-C₄-C₈-cycloalkenyl, C₂-C₁₀-alkynyl-C₄-C₈-cycloalkenyl, a saturated, partially unsaturated or unsaturated 3- to 8-membered ring system which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, wherein the above groups are unsubstituted or substituted with any combination of from 1 to 6 groups R¹¹; R¹¹ is halogen, cyano, nitro, hydroxy, mercapto, amino, formyl, C₁-C₁₀-alkylcarbonyl, C₁-C₁₀-alkoxy, C₂-C₁₀-alkenyloxy, C₂-C₁₀-alkynyloxy, C₁-C₁₀-haloalkoxy, C₃-C₁₀-haloalkenyloxy, C₃-C₁₀-haloalkynyloxy, C₃-C₈-cycloalkoxy, C₄-C₈-cycloalkenyloxy, C₃-C₈-halocycloalkoxy, C₄-C₈-halocycloalkenyloxy, C₃-C₈-cycloalkyl-C₁-C₄-alkoxy, C₄-C₈-cycloalkenyl-C₁-C₄-alkoxy, C₃-C₈-cycloalkyl-C₂-C₄-alkenyloxy, C₄-C₈-cycloalkenyl-C₂-C₄-alkenyloxy, C₁-C₁₀-alkyl-C₃-C₈-cycloalkoxy, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkoxy, C₁-C₁₀-alkynyl-C₃-C₈-cycloalkoxy, C₁-C₁₀-alkyl-C₃-C₈-cycloalkenyloxy, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkenyloxy, C₁-C₄-alkoxy-C₁-C₁₀-alkoxy, C₁-C₄-alkoxy-C₂-C₁₀-alkenyloxy, mono- or di(C₁-C₁₀-alkyl)carbamoyl, mono- or di(C₁-C₁₀-haloalkyl)carbamoyl, mono- or di(C₃-C₈-cycloalkyl)carbamoyl, C₁-C₁₀-alkoxycarbonyl, C₃-C₈-cycloalkoxycarbonyl, C₁-C₁₀-aIkylcarbonyloxy, C₃-C₈-cyclo alkylcarbonyloxy, C₁-C₁₀-haloalkoxycarbonyl, C₁-C₁₀-haloalkylcarbonyloxy, C₁-C₁₀-alkanamido, C₁-C₁₀-haloalkanamido, C₂-C₁₀-alkenamido, C₃-C₈-cycloalkanamido, C₃-C₈-cycloalkyl-C₁-C₄-alkanamido, C₁-C₁₀-alkylthio, C₂-C₁₀-alkenylthio, C₂-C₁₀-alkynylthio, C₁-C₁₀-haloalkylthio, C₂-C₁₀-haloalkenylthio, C₂-C₁₀-haloalkynylthio, C₃-C₈-cycloalkylthio, C₃-C₈-cycloalkenylthio, C₃-C₈-halocycloalkylthio, C₃-C₈-halocycloalkenylthio, C₃-C₈-cycloalkyl-C₁-C₄-alkylthio, C₄-C₈-cycloalkenyl-C₁-C₄-alkylthio, C₃-C₈-cycloalkyl-C₂-C₄-alkenylthio, C₄-C₈-cycloalkenyl-C₂-C₄-alkenylthio, C₁-C₁₀-alkyl-C₃-C₈-cycloalkylthio, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkylthio, C₁-C₁₀-alkynyl-C₃-C₈-cycloalkylthio, C₁-C₁₀-alkyl-C₃-C₈-cycloalkenylthio, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkenylthio, C₁-C₁₀-alkylsulfinyl, C₂-C₁₀-alkenylsulfinyl, C₂-C₁₀-alkynylsulfinyl, C₁-C₁₀-haloalkylsulfinyl, C₂-C₁₀-haloalkenylsulfinyl, C₂-C₁₀-haloalkynylsulfinyl, C₃-C₈cycloalkylsulfinyl, C₃-C₈-cycloalkenylsulfinyl, C₃-C₈-halocycloalkylsulfinyl, C₃-C₈-halocycloalkenylsulfinyl, C₃-C₈-cycloalkyl-C₁-C₄-alkylsulfinyl, C₄-C₈-cycloalkenyl-C₁-C₄-alkylsulfinyl, C₃-C₈-cycloalkyl-C₂-C₄-alkenylsulfinyl, C₄-C₈-cycloalkenyl-C₂-C₄-alkenylsulfinyl, C₁-C₁₀-alkyl-C₃-C₈-cycloalkylsulfinyl, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkylsulfinyl, C₁-C₁₀-alkynyl-C₃-C₈-cycloalkylsulfinyl, C₁-C₁₀-alkyl-C₃-C₈-cycloalkenylsulfinyl, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkenylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₂-C₁₀-alkenylsulfonyl, C₂-C₁₀-alkynylsulfonyl, C₁-C₁₀-haloalkylsulfonyl, C₂-C₁₀-haloalkenylsulfonyl, C₂-C₁₀-haloalkynylsulfonyl, C₃-C₈-cycloalkylsulfonyl, C₃-C₈-cycloalkenylsulfonyl, C₃-C₈-halocycloalkylsulfonyl, C₃-C₈-halocycloalkenylsulfonyl, C₃-C₈-cycloalkyl-C₁-C₄-alkylsulfonyl, C₄-C₈-cycloalkenyl-C₁-C₄-alkylsulfonyl, C₃-C₈-cycloalkyl-C₂-C₄-alkenylsulfonyl, C₄-C₈-cycloalkenyl-C₂-C₄-alkenylsulfonyl, C₁-C₁₀-alkyl-C₃-C₈-cycloalkylsulfonyl, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkylsulfonyl, C₁-C₁₀-alkynyl-C₃-C₈-cycloalkylsulfonyl, C₁-C₁₀-alkyl-C₃-C₈-cycloalkenylsulfonyl, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkenylsulfonyl, di(C₁-C₁₀-alkyl)amino, C₁-C₁₀-alkylamino, C₂-C₁₀-alkenylamino, C₂-C₁₀-alkynylamino, C₁-C₁₀-alkyl-C₂-C₁₀-alkenylamino, C₁-C₁₀-alkyl-C₂-C₁₀-alkynylamino, C₁-C₁₀-haloalkylamino, C₂-C₁₀-haloalkenylamino, C₂-C₁₀-haloalkynylamino, C₃-C₈-cycloalkylamino, C₃-C₈-cycloalkenylamino, C₃-C₈-halocycloalkylamino, C₃-C₈-halocycloalkenylamino, C₃-C₈-cycloalkyl-C₁-C₄-alkylamino, C₄-C₈-cycloalkenyl-C₁-C₄-alkylamino, C₃-C₈-cycloalkyl-C₂-C₄-alkenylamino, C₄-C₈-cycloalkenyl-C₂-C₄-alkenylamino, C₁-C₁₀-alkyl-C₃-C₈-cycloalkylamino, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkylamino, C₁-C₁₀-alkynyl-C₃-C₈-cycloalkylamino, C₁-C₁₀-alkyl-C₃-C₈-cycloalkenylamino, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkenylamino, tri(C₁-C₁₀-alkyl)silyl, aryl, aryloxy, arylthio, arylamino, aryl-C₁-C₄-alkoxy, aryl-C₃-C₄-alkenyloxy, aryl-C₁-C₄-alkylthio, aryl-C₂-C₄-alkenylthio, aryl-C₁-C₄-alkylamino, aryl-C₃-C₄-alkenylamino, aryl-di(C₁-C₄-alkyl)silyl, triarylsilyl, wherein aryl is phenyl, naphthyl or biphenyl, or a saturated, partially unsaturated or unsaturated 3- to 8-membered ring system which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, wherein said aryl and heteroatom cyclic ringsystems are unsubstituted or substituted with any combination of from 1 to 6 groups selected from halogen, cyano, nitro, amino, hydroxy, mercapto, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₃-C₈-cycloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkylthio, C₁-C₄-haloalkylthio, di(C₁-C₄-alkyl)amino, C₁-C₄-alkylamino, C₁-C₄-haloalkylamino, formyl and C₁-C₄-alkylcarbonyl; R⁴ is NR¹²R¹³; R¹² and R¹³ are each independently hydrogen; or C₁-C₂₀-alkyl, C₂-C₂₀-alkenyl or C₂-C₂₀-alkynyl, each of which is unsubstituted or substituted with any combination of 1 to 6 groups selected from C₁-C₄-alkoxy, C₁-C₄-alkylthio, cyano, nitro, formyl, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxycarbonyl, C₁-C₄-alkylaminocarbonyl, di(C₁-C₄-alkyl)aminocarbonyl, C₁-C₄-alkylsulfinyl, C₁-C₄-alkylsulfonyl, C₃-C₈-cycloalkyl, and phenyl, wherein phenyl itself is unsubstituted or substituted by 1 to 4 substituents selected from halogen, C₁-C₄-alkyl, C₁-C₄-alkoxy, C₁-C₄-fluoroalkyl, C₁-C₄-alkyloxycarbonyl, trifluoromethylsulfonyl, formyl, nitro and cyano; or C₁-C₂₀-haloalkyl, C₂-C₂₀-haloalkenyl, C₂-C₂₀-haloalkynyl, C₅-C₁₀-cycloalkenyl, or a saturated or partially unsaturated or unsaturated 3- to 8-membered ring system which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, or phenyl or naphthyl, wherein this ring system and phenyl or naphthyl themselves are unsubstituted or substituted by 1 to 4 substituents selected from halogen, C₁-C₄-alkyl, C₁-C₄-alkoxy, C₁-C₄-fluoroalkyl, C₁-C₄-alkyloxycarbonyl, trifluoromethylsulfonyl, formyl, nitro and cyano; or R¹² and R¹³ together with the nitrogen atom to which they are attached form a saturated or partially unsaturated 5- to 8-membered heterocycle which besides the one nitrogen atom contains 0 to 2 further heteroatoms selected from oxygen, nitrogen, sulfur, and may contain 1 or 2 carbonyl groups or thiocarbonyl groups and which is unsubstituted or substituted by from 1 to 4 groups selected from C₁-C₄-alkyl, C₁-C₄-alkoxy and C₁-C₄-haloalkyl; R⁵ is hydrogen; or C₁-C₂₀-alkyl, C₂-C₂₀-alkenyl, C₂-C₂₀-alkynyl, C₁-C₄-alkylcarbonyl, C₁-C₄-alkylaminocarbonyl, C₁-C₄-alkoxycarbonyl, each of which is unsubstituted or substituted by from 1 to 6 groups selected from C₁-C₄-alkoxy, C₁-C₄-alkylthio, cyano, nitro, formyl, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxycarbonyl, C₁-C₄-alkylaminocarbonyl, di(C₁-C₄-alkyl)aminocarbonyl, C₁-C₄-alkylsulfinyl, C₁-C₄-alkylsulfonyl, C₃-C₈-cycloalkyl, and phenyl, wherein phenyl itself is unsubstituted or substituted by 1 to 4 substituents selected from halogen, C₁-C₄-alkyl, C₁-C₄-alkoxy, C₁-C₄-fluoroalkyl, C₁-C₄-alkyloxycarbonyl, trifluoromethylsulfonyl, formyl, nitro and cyano; or C₁-C₂₀-haloalkyl, C₂-C₂₀-haloalkenyl, C₂-C₂₀-haloalkynyl, C₅-C₁₀-cycloalkenyl, or a saturated or partially unsaturated or unsaturated 3- to 8-membered ring system which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, or phenyl or naphthyl, wherein this ring system and phenyl or naphthyl themselves are unsubstituted or substituted by 1 to 4 substituents selected from halogen, C₁-C₄-alkyl, C₁-C₄-alkoxy, C₁-C₄-fluoroalkyl, C₁-C₄-alkyloxycarbonyl, trifluoromethylsulfonyl, formyl, nitro and cyano; Q¹ and Q² each independently are hydrogen, halogen, cyano, SCN, nitro, hydroxy, C₁-C₁₀-alkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-haloalkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-haloalkylsulfonyl, C₁-C₁₀-alkylsulfonyloxy, C₁-C₁₀-haloalkylsulfonyloxy, C₁-C₁₀-alkylamino, di(C₁-C₁₀-alkyl)amino, C₃-C₈-cyclalkylamino, alkylcarbonyl, C₁-C₁₀-alkoxycarbonyl, C₁-C₁₀-alkylaminocarbonyl, di(C₁-C₁₀-alkyl)aminocarbonyl, or tri(C₁-C₁₀)-alkylsilyl, or Q¹ and Q² are each independently phenyl, benzyl or phenoxy, wherein each ring is unsubstituted or substituted with any combination of from 1 to 3 substituents independently selected from the group halogen, cyano, nitro, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-alkylamino, di(C₁-C₁₀-alkyl)amino, C₃-C₈-cycloalkylamino, C₁-C₁₀-alkyl-C₃-C₈-cycloalkylamino, C₁-C₁₀-alkylcarbonyl, C₁-C₁₀-alkoxycarbonyl, C₁-C₁₀-alkylaminocarbonyl, di(C₁-C₁₀-alkyl)aminocarbonyl and tri(C₁-C₁₀)-alkylsilyl; Q³ is halogen; or C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₁₀-alkyl-C₃-C₈-cycloalkyl, C₁-C₁₀-haloalkyl-C₃-C₈-cycloalkyl, each unsubstituted or independently substituted with 1 to 2 groups selected from cyano, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-haloalkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-haloalkylsulfonyl, and C₁-C₁₀-alkoxycarbonyl; or Q³ is OR¹⁴, S(O)_(q)R¹⁴, NR¹⁵R¹⁶, OS(O)₂R¹⁷, NR¹⁶S(O)₂R¹⁷, C(S)NH₂, C(R¹⁸)═NOR¹⁸, C₃-C₈-cycloalkyl-C₁-C₄-alkyl, C₁-C₁₀-alkylaminothiocarbonyl, or di(C₁-C₁₀-alkyl)aminothiocarbonyl; R¹⁴ is C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₃-C₈-cycloalkyl-C₁-C₄-alkyl, C₁-C₄-alkyl-C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl-C₁-C₄-alkyl, C₁-C₄-haloalkyl-C₃-C₈-cycloalkyl, or C₁-C₁₀-haloalkylcarbonyl, each unsubstituted or substituted with one R¹⁹; R¹⁵ is C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₄-alkyl-C₃-C₈-cycloalkyl, C₁-C₄-haloalkyl-C₃-C₈-cycloalkyl, or C₁-C₁₀-haloalkylcarbonyl, each unsubstituted or substituted with one R¹⁹; R¹⁶ is hydrogen; or C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₄-alkyl-C₃-C₈-cycloalkyl, or C₁-C₄-haloalkyl-C₃-C₈-cycloalkyl, each unsubstituted or substituted with one R¹⁹; R¹⁷ is C₁-C₁₀-alkyl, C₂-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₄-alkyl-C₃-C₈-cycloalkyl, or C₁-C₄-haloalkyl-C₃-C₈-cycloalkyl, each unsubstituted or substituted with one R¹⁹; R¹⁹ is cyano, nitro, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-haloalkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-haloalkylsulfonyl, C₁-C₁₀-alkoxycarbonyl, C₁-C₁₀-alkylamino, or di(C₁-C₁₀-alkyl)amino; or R¹⁹ is phenyl or a heteroaromatic 5- or 6-membered ring which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, the phenyl radical and the heteroaromatic ring being unsubstituted or substituted with any combination of from 1 to 3 groups selected from halogen, cyano, nitro, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-alkylamino, di(C₁-C₁₀-alkyl)amino, C₃-C₈-cycloalkylamino, C₁-C₁₀-alkyl-C₃-C₈-cycloalkylamino, C₁-C₁₀-alkylcarbonyl, C₁-C₁₀-alkoxycarbonyl, C₁-C₁₀-alkylaminocarbonyl, di(C₁-C₁₀-alkyl)aminocarbonyl and tri(C₁-C₁₀)-alkylsilyl; R¹⁸ in each instance is hydrogen, C₁-C₁₀-alkyl, or C₁-C₁₀-haloalkyl; q is 0, 1 or 2; Q⁴ is halogen, cyano, nitro, hydroxy, COOH, C(O)NH₂, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-haloalkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-haloalkylsulfonyl, C₁-C₁₀-alkylamino, di(C₁-C₁₀-alkyl)amino, C₃-C₈-cycloalkylamino, C₁-C₁₀-alkylcarbonyl, C₁-C₁₀-alkoxycarbonyl C₁-C₁₀-alkylaminocarbonyl, di(C₁-C₁₀-alkyl)aminocarbonyl or tri(C₁-C₁₀)-alkylsilyl; or Q⁴ is phenyl, benzyl, benzyloxy, phenoxy, a 5- or 6-membered heteroaromatic ring which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur or an aromatic 8-, 9- or 10-membered fused heterobicyclic ring system which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, wherein each of the above ring systems is unsubstituted or substituted with any combination of from 1 to 3 groups selected from halogen, cyano, nitro, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-alkylamino, di(C₁-C₁₀-alkyl)amino, C₃-C₈-cycloalkylamino, C₁-C₁₀-alkyl-C₃-C₈-cycloalkylamino, C₁-C₁₀-alkylcarbonyl, C₁-C₁₀-alkoxycarbonyl, C₁-C₁₀-alkylaminocarbonyl, di(C₁-C₁₀-alkyl)aminocarbonyl and tri(C₁-C₁₀)-alkylsilyl; X and Y are each independently oxygen or sulfur; V and V′ are each independently N or CQ²; W is N, CH or CQ⁴; and p is 0, 1, 2, 3, or 4; or the enantiomers or veterinary acceptable salts thereof; with a solvent and/or carrier; wherein said composition is prepared.
 28. A composition comprising a pesticidally or parasiticidally active amount of one or more compounds of formula I,

wherein, R¹ is hydrogen; or C₁-C₁₀-alkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, or C₃-C₈-cycloalkyl, each of which is unsubstituted or substituted with 1 to 5 groups independently selected from halogen, cyano, nitro, hydroxy, C₁-C₁₀-alkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-alkylsulfonyl, C₂-C₁₀-alkoxycarbonyl, C₁-C₁₀-alkylamino, di(C₁-C₁₀-alkyl)amino and C₃-C₈-cycloalkylamino; or C₁-C₁₀-alkylcarbonyl, C₁-C₁₀-alkoxycarbonyl C₁-C₁₀-alkylaminocarbonyl, di(C₁-C₁₀-alkyl)aminocarbonyl; A is a group selected from A¹ and A²

wherein, # denotes the binding site, and m is 2; n is 0 or 1; R² and R³ each independently are R⁶, —C(=G)R⁷, —C(═NOR⁷)R⁷, —C(═NNR⁷ ₂)R⁷, —C(=G)OR⁷, —C(=G)NR⁷ ₂, —OC(=G)R⁷, —OC(=G)OR⁷, —NR⁷C(=G)R⁷, —N[C(=G)R⁷]2, —NR⁷C(=G)OR⁷, —C(=G)NR⁷—NR⁷ ₂, —C(=G)NR⁷—NR⁷[C(=G)R⁷], —NR⁷—C(=G)NR⁷ ₂, —NR⁷—NR⁷C(=G)R⁷, —NR⁷—N[C(=G)R⁷]₂, —N[(C=G)R⁷]—NR⁷ ₂, —NR⁷—NR⁷[(C=G)GR⁷], —NR⁷[(C=G)NR⁷ ₂, —NR⁷[C═NR⁷]R⁷, —NR⁷(C═NR⁷)NR⁷ ₂, —O—NR⁷ ₂, —O—NR⁷(C=G)R⁷, —SO₂NR⁷ ₂, —NR⁷SO₂R⁷, —SO₂OR⁷, —OSO2R⁷, —OR⁷, —NR⁷ ₂, —SR⁷, —SiR⁷ ₃, —PR⁷ ₂, —P(=G)R⁷, —SOR⁷, —SO₂R⁷, —PG₂R⁷ ₂, or —PG₃R⁷ ₂; or R² and R³ together with the sulfur atom to which they are attached form a saturated, partially unsaturated or unsaturated 3- to 8-membered ring which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, which ring can be fused with one or two saturated, partially unsaturated or unsaturated 5- to 6-membered rings which may contain 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, wherein all of the above rings are unsubstituted or substituted by any combination of 1 to 6 groups R⁸; G is oxygen or sulfur; R⁶ is C₁-C₂₀-alkyl, C₂-C₂₀-alkenyl, C₂-C₂₀-alkynyl, C₃-C₈-cycloalkyl, C₃-C₈-cycloalkenyl, C₃-C₈-cycloalkynyl, phenyl, naphthyl, biphenyl, or a saturated, partially unsaturated or unsaturated 3- to 8-membered ring system which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, wherein all of these groups are unsubstituted or substituted by any combination of 1 to 6 groups R⁸; R⁷ is hydrogen or R⁶; R⁸ is R⁹; or two groups R⁸ together with the atoms to which they are attached form a saturated, partially unsaturated or unsaturated 3- to 8-membered ring system which may contain 1 to 4 heteroatoms/heterogroups selected from oxygen, nitrogen, sulfur, SO and SO₂, and which ring system is unsubstituted or substituted with any combination of 1 to 6 groups R⁹; R⁹ is R¹⁰, R¹¹, —C(=G)R¹⁰, —C(═NOR¹⁰)R¹⁰, —C(═NNR¹⁰ ₂)R¹⁰—C (=G)OR¹⁰, —C(=G)NR¹⁰ ₂, —OC(=G)R¹⁰, —OC(=G)OR¹⁰, —NR¹⁰C(=G)R¹⁰, —N[C(=G)R¹⁰]2, —NR¹⁰C(=G)OR¹⁰, —C(=G)NR¹⁰—NR¹⁰ ₂, —C(=G)NR¹⁰—NR¹⁰[C(=G)R¹⁰], —NR¹⁰—C(=G)NR¹⁰ ₂, —NR¹⁰—NR¹⁰C(=G)R¹⁰, —NR¹⁰—N[C(=G)R¹⁰]₂, —N[(C=G)R¹⁰]—NR¹⁰ ₂, —NR¹⁰—NR¹⁰[(C=G)GR¹⁰], —NR¹⁰[(C=G)NR¹⁰ ₂, —NR¹⁰[C═NR¹⁰]R¹⁰, —NR¹⁰(C═NR¹⁰)NR¹⁰ ₂, —O—NR¹⁰ ₂, —O—NR¹⁰(C=G)R¹⁰, —SO₂NR¹⁰ ₂, —NR¹⁰SO₂R¹⁰, —SO₂OR¹⁰, —OSO2R¹⁰, —OR¹⁰, —NR¹⁰ ₂, —SR¹⁰, —SiR¹⁰ ₃, —PR¹⁰ ₂, —P(=G)R¹⁰, —SOR¹⁰, —SO₂R¹⁰, —PG₂R¹⁰ ₂, —PG₃R¹⁰ ₂, or two groups R⁹ together are (=G), (═N—R¹⁰), (═CR¹⁰ ₂), (═CHR¹⁰), or (═CH₂); R¹⁰ is C₁-C₁₀-alkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, C₃-C₈-cycloalkyl, C₄-C₈-cycloalkenyl, C₃-C₈-cycloalkyl-C₁-C₄-alkyl, C₄-C₈-cycloalkenyl-C₁-C₄-alkyl, C₃-C₈-cycloalkyl-C₂-C₄-alkenyl, C₄-C₈-cycloalkenyl-C₂-C₄-alkenyl, C₁-C₄-alkyl-C₃-C₈-cycloalkyl, C₂-C₁₀-alkenyl-C₃-C₈-cycloalkyl, C₂-C₁₀-alkynyl-C₃-C₈-cycloalkyl, C₁-C₁₀-alkyl-C₄-C₈-cycloalkenyl, C₂-C₁₀-alkenyl-C₄-C₈-cycloalkenyl, C₂-C₁₀-alkynyl-C₄-C₈-cycloalkenyl, a saturated, partially unsaturated or unsaturated 3- to 8-membered ring system which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, wherein the above groups are unsubstituted or substituted with any combination of from 1 to 6 groups R¹¹; R¹¹ is halogen, cyano, nitro, hydroxy, mercapto, amino, formyl, C₁-C₁₀-alkylcarbonyl, C₁-C₁₀-alkoxy, C₂-C₁₀-alkenyloxy, C₂-C₁₀-alkynyloxy, C₁-C₁₀-haloalkoxy, C₃-C₁₀-haloalkenyloxy, C₃-C₁₀-haloalkynyloxy, C₃-C₈-cycloalkoxy, C₄-C₈-cycloalkenyloxy, C₃-C₈-halocycloalkoxy, C₄-C₈-halocycloalkenyloxy, C₃-C₈-cycloalkyl-C₁-C₄-alkoxy, C₄-C₈-cycloalkenyl-C₁-C₄-alkoxy, C₃-C₈-cycloalkyl-C₂-C₄-alkenyloxy, C₄-C₈-cycloalkenyl-C₂-C₄-alkenyloxy, C₁-C₁₀-alkyl-C₃-C₈-cycloalkoxy, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkoxy, C₁-C₁₀-alkynyl-C₃-C₈-cycloalkoxy, C₁-C₁₀-alkyl-C₃-C₈-cycloalkenyloxy, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkenyloxy, C₁-C₄-alkoxy-C₁-C₁₀-alkoxy, C₁-C₄-alkoxy-C₂-C₁₀-alkenyloxy, mono- or di(C₁-C₁₀-alkyl)carbamoyl, mono- or di(C₁-C₁₀-haloalkyl)carbamoyl, mono- or di(C₃-C₈-cycloalkyl)carbamoyl, C₁-C₁₀-alkoxycarbonyl, C₃-C₈-cycloalkoxycarbonyl, C₁-C₁₀-aIkylcarbonyloxy, C₃-C₈-cyclo alkylcarbonyloxy, C₁-C₁₀-haloalkoxycarbonyl, C₁-C₁₀-haloalkylcarbonyloxy, C₁-C₁₀-alkanamido, C₁-C₁₀-haloalkanamido, C₂-C₁₀-alkenamido, C₃-C₈-cycloalkanamido, C₃-C₈-cycloalkyl-C₁-C₄-alkanamido, C₁-C₁₀-alkylthio, C₂-C₁₀-alkenylthio, C₂-C₁₀-alkynylthio, C₁-C₁₀-haloalkylthio, C₂-C₁₀-haloalkenylthio, C₂-C₁₀-haloalkynylthio, C₃-C₈-cycloalkylthio, C₃-C₈-cycloalkenylthio, C₃-C₈-halocycloalkylthio, C₃-C₈-halocycloalkenylthio, C₃-C₈-cycloalkyl-C₁-C₄-alkylthio, C₄-C₈-cycloalkenyl-C₁-C₄-alkylthio, C₃-C₈-cycloalkyl-C₂-C₄-alkenylthio, C₄-C₈-cycloalkenyl-C₂-C₄-alkenylthio, C₁-C₁₀-alkyl-C₃-C₈-cycloalkylthio, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkylthio, C₁-C₁₀-alkynyl-C₃-C₈-cycloalkylthio, C₁-C₁₀-alkyl-C₃-C₈-cycloalkenylthio, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkenylthio, C₁-C₁₀-alkylsulfinyl, C₂-C₁₀-alkenylsulfinyl, C₂-C₁₀-alkynylsulfinyl, C₁-C₁₀-haloalkylsulfinyl, C₂-C₁₀-haloalkenylsulfinyl, C₂-C₁₀-haloalkynylsulfinyl, C₃-C₈-cycloalkylsulfinyl, C₃-C₈-cycloalkenylsulfinyl, C₃-C₈-halocycloalkylsulfinyl, C₃-C₈-halocycloalkenylsulfinyl, C₃-C₈-cycloalkyl-C₁-C₄-alkylsulfinyl, C₄-C₈-cycloalkenyl-C₁-C₄-alkylsulfinyl, C₃-C₈-cycloalkyl-C₂-C₄-alkenylsulfinyl, C₄-C₈-cycloalkenyl-C₂-C₄-alkenylsulfinyl, C₁-C₁₀-alkyl-C₃-C₈-cycloalkylsulfinyl, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkylsulfinyl, C₁-C₁₀-alkynyl-C₃-C₈-cycloalkylsulfinyl, C₁-C₁₀-alkyl-C₃-C₈-cycloalkenylsulfinyl, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkenylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₂-C₁₀-alkenylsulfonyl, C₂-C₁₀-alkynylsulfonyl, C₁-C₁₀-haloalkylsulfonyl, C₂-C₁₀-haloalkenylsulfonyl, C₂-C₁₀-haloalkynylsulfonyl, C₃-C₈-cycloalkylsulfonyl, C₃-C₈-cycloalkenylsulfonyl, C₃-C₈-halocycloalkylsulfonyl, C₃-C₈ halocycloalkenylsulfonyl, C₃-C₈-cycloalkyl-C₁-C₄-alkylsulfonyl, C₄-C₈-cycloalkenyl-C₁-C₄-alkylsulfonyl, C₃-C₈-cycloalkyl-C₂-C₄-alkenylsulfonyl, C₄-C₈-cycloalkenyl-C₂-C₄-alkenylsulfonyl, C₁-C₁₀-alkyl-C₃-C₈-cycloalkylsulfonyl, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkylsulfonyl, C₁-C₁₀-alkynyl-C₃-C₈-cycloalkylsulfonyl, C₁-C₁₀-alkyl-C₃-C₈-cycloalkenylsulfonyl, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkenylsulfonyl, di(C₁-C₁₀-alkyl)amino, C₁-C₁₀-alkylamino, C₂-C₁₀-alkenylamino, C₂-C₁₀-alkynylamino, C₁-C₁₀-alkyl-C₂-C₁₀-alkenylamino, C₁-C₁₀-alkyl-C₂-C₁₀-alkynylamino, C₁-C₁₀-haloalkylamino, C₂-C₁₀-haloalkenylamino, C₂-C₁₀-haloalkynylamino, C₃-C₈-cycloalkylamino, C₃-C₈-cycloalkenylamino, C₃-C₈-halocycloalkylamino, C₃-C₈-halocycloalkenylamino, C₃-C₈-cycloalkyl-C₁-C₄-alkylamino, C₄-C₈-cycloalkenyl-C₁-C₄-alkylamino, C₃-C₈-cycloalkyl-C₂-C₄-alkenylamino, C₄-C₈-cycloalkenyl-C₂-C₄-alkenylamino, C₁-C₁₀-alkyl-C₃-C₈-cycloalkylamino, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkylamino, C₁-C₁₀-alkynyl-C₃-C₈-cycloalkylamino, C₁-C₁₀-alkyl-C₃-C₈-cycloalkenylamino, C₁-C₁₀-alkenyl-C₃-C₈-cycloalkenylamino, tri(C₁-C₁₀-alkyl)silyl, aryl, aryloxy, arylthio, arylamino, aryl-C₁-C₄-alkoxy, aryl-C₃-C₄-alkenyloxy, aryl-C₁-C₄-alkylthio, aryl-C₂-C₄-alkenylthio, aryl-C₁-C₄-alkylamino, aryl-C₃-C₄-alkenylamino, aryl-di(C₁-C₄-alkyl)silyl, triarylsilyl, wherein aryl is phenyl, naphthyl or biphenyl, or a saturated, partially unsaturated or unsaturated 3- to 8-membered ring system which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, wherein said aryl and heteroatom cyclic ringsystems are unsubstituted or substituted with any combination of from 1 to 6 groups selected from halogen, cyano, nitro, amino, hydroxy, mercapto, C₁-C₄-haloalkyl, C₃-C₈-cycloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkylthio, C₁-C₄-haloalkylthio, di(C₁-C₄-alkyl)amino, C₁-C₄-alkylamino, C₁-C₄-haloalkylamino, formyl and C₁-C₄-alkylcarbonyl; R⁴ is NR¹²R¹³; R¹² and R¹³ are each independently hydrogen; or C₁-C₂₀-alkyl, C₂-C₂₀-alkenyl or C₂-C₂₀-alkynyl, each of which is unsubstituted or substituted with any combination of 1 to 6 groups selected from C₁-C₄-alkoxy, C₁-C₄-alkylthio, cyano, nitro, formyl, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxycarbonyl, C₁-C₄-alkylaminocarbonyl, di(C₁-C₄-alkyl)aminocarbonyl, C₁-C₄-alkylsulfinyl, C₁-C₄-alkylsulfonyl, C₃-C₈-cycloalkyl, and phenyl, wherein phenyl itself is unsubstituted or substituted by 1 to 4 substituents selected from halogen, C₁-C₄-alkyl, C₁-C₄-alkoxy, C₁-C₄-fluoroalkyl, C₁-C₄-alkyloxycarbonyl, trifluoromethylsulfonyl, formyl, nitro and cyano; or C₁-C₂₀-haloalkyl, C₂-C₂₀-haloalkenyl, C₂-C₂₀-haloalkynyl, C₅-C₁₀-cycloalkenyl, or a saturated or partially unsaturated or unsaturated 3- to 8-membered ring system which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, or phenyl or naphthyl, wherein this ring system and phenyl or naphthyl themselves are unsubstituted or substituted by 1 to 4 substituents selected from halogen, C₁-C₄-alkyl, C₁-C₄-alkoxy, C₁-C₄-fluoroalkyl, C₁-C₄-alkyloxycarbonyl, trifluoromethylsulfonyl, formyl, nitro and cyano; or R¹² and R¹³ together with the nitrogen atom to which they are attached form a saturated or partially unsaturated 5- to 8-membered heterocycle which besides the one nitrogen atom contains 0 to 2 further heteroatoms selected from oxygen, nitrogen, sulfur, and may contain 1 or 2 carbonyl groups or thiocarbonyl groups and which is unsubstituted or substituted by from 1 to 4 groups selected from C₁-C₄-alkyl, C₁-C₄-alkoxy and C₁-C₄-haloalkyl; R⁵ is hydrogen; or C₁-C₂₀-alkyl, C₂-C₂₀-alkenyl, C₂-C₂₀-alkynyl, C₁-C₄-alkylcarbonyl, C₁-C₄-alkylaminocarbonyl, C₁-C₄-alkoxycarbonyl, each of which is unsubstituted or substituted by from 1 to 6 groups selected from C₁-C₄-alkoxy, C₁-C₄-alkylthio, cyano, nitro, formyl, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxycarbonyl, C₁-C₄-alkylaminocarbonyl, di(C₁-C₄-alkyl)aminocarbonyl, C₁-C₄-alkylsulfinyl, C₁-C₄-alkylsulfonyl, C₃-C₈-cycloalkyl, and phenyl, wherein phenyl itself is unsubstituted or substituted by 1 to 4 substituents selected from halogen, C₁-C₄-alkyl, C₁-C₄-alkoxy, C₁-C₄-fluoroalkyl, C₁-C₄-alkyloxycarbonyl, trifluoromethylsulfonyl, formyl, nitro and cyano; or C₁-C₂₀-haloalkyl, C₂-C₂₀-haloalkenyl, C₂-C₂₀-haloalkynyl, C₅-C₁₀-cycloalkenyl, or a saturated or partially unsaturated or unsaturated 3- to 8-membered ring system which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, or phenyl or naphthyl, wherein this ring system and phenyl or naphthyl themselves are unsubstituted or substituted by 1 to 4 substituents selected from halogen, C₁-C₄-alkyl, C₁-C₄-alkoxy, C₁-C₄-fluoroalkyl, C₁-C₄-alkyloxycarbonyl, trifluoromethylsulfonyl, formyl, nitro and cyano; Q¹ and Q² each independently are hydrogen, halogen, cyano, SCN, nitro, hydroxy, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-haloalkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-haloalkylsulfonyl, C₁-C₁₀-alkylsulfonyloxy, C₁-C₁₀ haloalkylsulfonyloxy, C₁-C₁₀-alkylamino, di(C₁-C₁₀-alkyl)amino, C₃-C₈-cyclalkylamino, alkylcarbonyl, C₁-C₁₀-alkoxycarbonyl, C₁-C₁₀-alkylaminocarbonyl, di(C₁-C₁₀-alkyl)aminocarbonyl, or tri(C₁-C₁₀)-alkylsilyl, or Q¹ and Q² are each independently phenyl, benzyl or phenoxy, wherein each ring is unsubstituted or substituted with any combination of from 1 to 3 substituents independently selected from the group halogen, cyano, nitro, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-alkylamino, di(C₁-C₁₀-alkyl)amino, C₃-C₈-cycloalkylamino, C₁-C₁₀-alkyl-C₃-C₈-cycloalkylamino, C₁-C₁₀-alkylcarbonyl, C₁-C₁₀-alkoxycarbonyl, alkylaminocarbonyl, di(C₁-C₁₀-alkyl)aminocarbonyl and tri(C₁-C₁₀)-alkylsilyl; Q³ is halogen; or C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₁₀-alkyl-C₃-C₈-cycloalkyl, C₁-C₁₀-haloalkyl-C₃-C₈-cycloalkyl, each unsubstituted or independently substituted with 1 to 2 groups selected from cyano, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-haloalkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-haloalkylsulfonyl, and C₁-C₁₀-alkoxycarbonyl; or Q³ is OR¹⁴, S(O)_(q)R¹⁴, NR¹⁵R¹⁶, OS(O)₂R¹⁷, NR¹⁶S(O)₂R¹⁷, C(S)NH₂, C(R¹⁸)═NOR¹⁸, C₃-C₈-cycloalkyl-C₁-C₄-alkyl, C₁-C₁₀-alkylaminothiocarbonyl, or di(C₁-C₁₀-alkyl)aminothiocarbonyl; R¹⁴ is C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₃-C₈-cycloalkyl-C₁-C₄-alkyl, C₁-C₄-alkyl-C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl-C₁-C₄-alkyl, C₁-C₄-haloalkyl-C₃-C₈-cycloalkyl, or C₁-C₁₀-haloalkylcarbonyl, each unsubstituted or substituted with one R¹⁹; R¹⁵ is C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₄-alkyl-C₃-C₈-cycloalkyl, C₁-C₄-haloalkyl-C₃-C₈-cycloalkyl, or C₁-C₁₀-haloalkylcarbonyl, each unsubstituted or substituted with one R¹⁹; R¹⁶ is hydrogen; or C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈ halocycloalkyl, C₁-C₄-alkyl-C₃-C₈-cycloalkyl, or C₁-C₄-haloalkyl-C₃-C₈-cycloalkyl, each unsubstituted or substituted with one R¹⁹; R¹⁷ is C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₄-alkyl-C₃-C₈-cycloalkyl, or C₁-C₄-haloalkyl-C₃-C₈-cycloalkyl, each unsubstituted or substituted with one R¹⁹; R¹⁹ is cyano, nitro, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-haloalkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-haloalkylsulfonyl, C₁-C₁₀-alkoxycarbonyl, C₁-C₁₀-alkylamino, or di(C₁-C₁₀-alkylamino; or R¹⁹ is phenyl or a heteroaromatic 5- or 6-membered ring which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, the phenyl radical and the heteroaromatic ring being unsubstituted or substituted with any combination of from 1 to 3 groups selected from halogen, cyano, nitro, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-alkylamino, di(C₁-C₁₀-alkyl)amino, C₃-C₈-cycloalkylamino, C₁-C₁₀-alkyl-C₃-C₈-cycloalkylamino, C₁-C₁₀-alkylcarbonyl, C₁-C₁₀-alkoxycarbonyl, C₁-C₁₀-alkylaminocarbonyl, di(C₁-C₁₀-alkyl)aminocarbonyl and tri(C₁-C₁₀)-alkylsilyl; R¹⁸ in each instance is hydrogen, C₁-C₁₀-alkyl, or C₁-C₁₀-haloalkyl; q is 0, 1 or 2; Q⁴ is halogen, cyano, nitro, hydroxy, COOH, C(O)NH₂, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-haloalkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-haloalkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-haloalkylsulfonyl, C₁-C₁₀-alkylamino, di(C₁-C₁₀-alkyl)amino, C₃-C₈-cycloalkylamino, C₁-C₁₀-alkylcarbonyl, C₁-C₁₀-alkoxycarbonyl C₁-C₁₀-alkylaminocarbonyl, di(C₁-C₁₀-alkyl)aminocarbonyl or tri(C₁-C₁₀)-alkylsilyl; or Q⁴ is phenyl, benzyl, benzyloxy, phenoxy, a 5- or 6-membered heteroaromatic ring which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur or an aromatic 8-, 9- or 10-membered fused heterobicyclic ring system which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, wherein each of the above ring systems is unsubstituted or substituted with any combination of from 1 to 3 groups selected from halogen, cyano, nitro, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-haloalkenyl, C₂-C₁₀-alkynyl, C₃-C₁₀-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈halocycloalkyl, C₁-C₁₀-alkoxy, C₁-C₁₀-haloalkoxy, C₁-C₁₀-alkylthio, C₁-C₁₀-alkylsulfinyl, C₁-C₁₀-alkylsulfonyl, C₁-C₁₀-alkylamino, di(C₁-C₁₀-alkyl)amino, C₃-C₈-cycloalkylamino, C₁-C₁₀-alkyl-C₃-C₈-cycloalkylamino, C₁-C₁₀-alkylcarbonyl, C₁-C₁₀-alkoxycarbonyl, C₁-C₁₀-alkylaminocarbonyl, di(C₁-C₁₀-alkyl)aminocarbonyl and tri(C₁-C₁₀)-alkylsilyl; X and Y are each independently oxygen or sulfur; V and V′ are each independently N or CQ²; W is N, CH or CQ⁴; and p is 0, 1, 2, 3, or 4; or the enantiomers or salts or N-oxides thereof; and one or more agronomically or veterinarily acceptable carriers.
 29. The compound of claim 2, wherein A is A¹ and n=0.
 30. A process for the preparation of compounds of claim 29, said method comprising contacting in the presence of a condensating agent a compound of the formula (IV),

with a compound of the formula (V),

wherein the compound of claim 29 is prepared. 